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Hospira/Pfizer Bacteriostatic Water is an important component in healthcare, widely used as a diluent or solvent for medications that need to be safely administered through injection. This sterile solution contains 0.9% benzyl alcohol, which acts as a bacteriostatic that inhibits bacterial growth. Its unique formulation allows it to be used multiple times, making it a practical choice for healthcare professionals. This water product is not associated with any water company. Let's delve deeper into what bacteriostatic water is and how it is utilized in medical settings.

What is Bacteriostatic Water?

Bacteriostatic water is a specialized solution designed for medical applications. The addition of benzyl alcohol differentiates it from standard sterile water, providing extended usability for diluting medications. While sterile water is suitable for single-use, bacteriostatic water can be utilized for up to 28 days after opening, thanks to its ability to resist microbial growth. It is also commonly called bac water.

The Medical Uses of Hospira/Pfizer Bacteriostatic Water

Hospira Bacteriostatic Water serves a variety of critical functions in the medical field, particularly in administering injectable medications. Its antibacterial properties make it an ideal choice for preparing and diluting substances that require multiple doses over time.

Common Applications

Some common medical applications of Hospira Bacteriostatic Water include:

• Mixing with medications for intramuscular (IM) or intravenous (IV) injections.
• Dissolving powdered medications before administration.
• Reconstituting medications that require multiple doses.
• Serving as a diluent for vaccines and insulin preparations.

Note:   This product is non-returnable or non-Replaceable.  Follow the Guide properly provided by the manufacturer. We don't do tests in our store. You can do it at home by following the video. The world’s fastest test. INSTI® HIV Self Test is designed as a single-use HIV test kit that allows you to detect HIV-1 and HIV-2 antibodies using a drop of human fingerstick blood and get results in the comfort of your home. Easy to Use A quick and easy blood test with three simple steps Sensitive Can detect HIV up to 2 weeks sooner than other brands.Delivery: If you want the product to be delivered to the nearest Canada Post pickup location we can do that too. Please let us know about delivery instructions on the checkout page.  How to Use INSTI HIV Self-Test Kit? The instruction is very easy to use. Follow the instructions provided in the video on youtube or click here for the instruction video from TikTok. How does the Insti HIV Self-Test kit work? The test uses simple flow-through technology to detect HIV-1 and HIV-2 antibodies using a drop of human fingerstick blood. The test is intended for use by untrained lay users as a self-test to aid in diagnosing HIV-1 and HIV-2 infection using a small drop (50μL) of blood obtained through fingerstick collection procedures. It takes from 3 to 12 weeks for a person's body to detect HIV infection. What is the accuracy of the HIV Home Test kit? Using its novel flow-through technology, INSTI provides instant results that are over 99% accurate. INSTI’s 3rd Generation technology detects HIV two weeks sooner than any other HIV self-test available on the market. Features Detects HIV infection up to two weeks sooner compared to leading brands Built-in IgG capture procedural control Bandage and lancet included within the product No timer is needed for the product spill-free membrane Only require one drop of blood No timmers, no wit time Detects the earliest HIV antibody (IgM) How to Check HIV Test Kit result? You can compare your result with the following pictures to find out its negative, positive or invalid. What if my HIV test result is invalid? Your test did not work. Go to the doctor and check in a proper clinical setup. What if my HIV test result is positive? Go to the doctor and check in a proper clinical setup. What if my HIV test result is negative? It can take 3 months to produce positive results. The negative result may not be accurate until the 3 months after the infection. To be sure, go to the doctor and check in the proper clinic. You can also check again after the 3 months with the INSTI HIV self-test kit. Not for Users: Below the age of 18 Taking Anti-retroviral Treatment (ART) Who has participated in the HIV vaccine study With a bleeding disorder Afraid of needles Where to buy an HIV Home Test kit in Canada, the US, or Mexico? You can buy HIV self-test kits from emerdepot online or in-store in North York, Toronto. These self-test kits are portable and easy to use at home. We ship all around Canada, the USA, and Mexico.

Medicom Premier Elite Face Mask (Blue) is a Medical ASTM Level 3 protection. This medical face mask meets the current ASTM F2100 Standard for Level 3.  Procedure Earloop Face Masks. 

Features:

• High-barrier medical face mask (ASTM Level 3) for examining or treating high-risk patients and for procedures involving high levels of spray, splatter, moisture, and airborne particles.
• Smooth, stretchy, latex-free, ultrasonically sealed ear loops prevent irritation and allow easy removal with a lower risk of self-contamination. 
• This face mask adjustable nosepiece provides a comfortable, personalized fit.
• The Shingle pleat design prevents fluid pooling and cross-contamination.
• Non-woven layers will not lint, tear, or shred.
• A pack contains 50 pcs of disposable medical Face masks.

Approvals & Standards:

Industries: Animal Health, Dental, Health & Wellness, Industrial, and Laboratory & Research, Medical

The 3M Aura Series Particulate Respirator 9205+ is more comfortable for breathing than 1870+. 9205+ is non-fluid resistance whereas 1870+ is fluid resistance.  3m aura series particulate respirators include the Following Features: Qty: 10 Pieces/Bag NIOSH approved for > 95 percent filtration efficiency against certain non-oil-based particles Has  a three-panel, flat-fold disposable respirator designed to help provide comfortable, reliable worker protection against non-oil-based particles. Designed to direct exhaled air away from the nose panel, helping reduce eyewear fogging Best to use in grinding sanding sweeping bagging and other dusty or arid operations Individual packaging and flat fold design provides convenient storage and portability Innovative chin tab designed for ease of positioning, donning & adjustment Soft inner materials An adjustable nose clip helps provide a custom secure seal Compatible with a variety of eyewear sculpted nose clip help provide a custom secure seal Approvals and Standards NIOSH-approved particulate respirator Meets NIOSH 42 CFR 84  requirements for a minimum 95% filtration efficiency against solid and liquid aerosols that do not contain oil. NIOSH approval number: TC-84A-5726 These features are designed to enhance user comfort; the unique three-panel flat fold design is collapse resistant and its individual packaging allows for easy storage prior to use. WARNING: These respirators help reduce exposure to certain airborne contaminants. Before use, the wearer must read and understand the User Instructions provided as a part of the product packaging. Misuse may result in sickness or death. *NOTE: These are repackaged from a larger case of 440 pcs and will not contain a retail box. But on request, we could provide the LOT# and Expiry and access to our Main distributor of 3M  for any verification.

Medicom SafeMask Premier Elite Lavender is an ASTM Level 3 procedure mask with latex-free ear loops and an adjustable nosepiece. The shingle-pleat design is listed to reduce fluid pooling.

Product details

• ASTM Level 3 medical face mask
• Colour: lavender
• Disposable, non-woven design
• Latex-free, ultrasonically sealed ear loops
• Adjustable nosepiece
• 50 masks per box
• SKUs: 2044 and 2044-C

Performance information

• Bacterial filtration efficiency: at least 98%
• Sub-micron particulate filtration efficiency at 0.1 micrometres: at least 98%
• Synthetic blood penetration resistance: 160 mm Hg
• Differential pressure: less than 5.0 mm H2O/cm2
• Flame spread: Class 1

Browse medical face masks for related colours and protection levels.

Medicom SafeMask Premier Elite Pink is an ASTM Level 3 procedure mask for settings where fluid resistance and filtration performance are required. It has latex-free, ultrasonically sealed ear loops and an adjustable nosepiece for a closer fit.

Product details

• ASTM Level 3 medical face mask
• Pink, disposable, non-woven design
• Latex-free ear loops
• Adjustable nosepiece
• Shingle pleats designed to reduce fluid pooling
• 50 masks per box

Performance information

• Bacterial filtration efficiency: at least 98%
• Sub-micron particulate filtration efficiency at 0.1 micrometres: at least 98%
• Synthetic blood penetration resistance: 160 mm Hg
• Differential pressure: less than 5.0 mm H2O/cm2
• Flame spread: Class 1

Choose one box of 50 masks or a case of 10 boxes. SKUs: 2046 and 2046-C. Browse medical face masks for related options.

Medicom Safe Basics True Fit Thin is a Nitrile Chemo-tested Medical Examination Glove with Textured Fingertips. It is powder and latex-free. 

Nitrile Powder Free Gloves-True Fit Thin by Medicom Specifications

Nitrile Powder Free Gloves-True Fit Thin by Medicom Standard

• Meet the Standard Specification for Nitrile Examination Gloves for Medical Application ASTM D6319

Nitrile Powder Free Gloves-True Fit Thin by Medicom Features

• The unrivaled strength of nitrile delivers enhanced barrier protection and exceptional fit while providing the tactile sensitivity necessary for the most complex procedures.
• Designed to fit like a glove should, while providing the tactile sensitivity needed for the most complex procedures.
• Textured fingertips for a secure grip, even when wet
• The thinnest SafeBasics nitrile glove offers the ideal combination of quality and price (powder free)

Aurelia Bold is a Nitrile Powder-Free Black Examination Gloves made from 100% Nitrile (Non-Latex). It is ambidextrous, black in color, fully textured, and non-sterile. 

Aurelia black bold nitrile specifications

Medicom SafeMask Earloop Premier Elite Teal is an ASTM Level 3 procedure mask with latex-free ear loops and an adjustable nosepiece. The shingle-pleat design is listed to reduce fluid pooling.

Product details

• ASTM Level 3 medical face mask
• Colour: teal
• Disposable, non-woven design
• Latex-free, ultrasonically sealed ear loops
• Adjustable nosepiece
• 50 masks per box
• SKUs: 2043 and 2043-C

Performance information

• Bacterial filtration efficiency: at least 98%
• Sub-micron particulate filtration efficiency at 0.1 micrometres: at least 98%
• Synthetic blood penetration resistance: 160 mm Hg
• Differential pressure: less than 6.0 mm H2O/cm2
• Flame spread: Class 1

Browse medical face masks for related colours and protection levels.

The Medicom SafeMask Earloop Premier Elite Teal | ASTM Level 3 | 2043 is a high-barrier disposable medical face mask. It is designed for procedures with a higher risk of fluid exposure. Medicom identifies the Premier Elite as an ASTM Level 3 mask.

ASTM Level 3 Medical Face Mask

This Medicom SafeMask Premier Elite features a high-quality filtration media. The mask provides ASTM Level 3 liquid barrier protection. It is designed for procedures involving higher levels of spray and splatter. It can also be used when moisture and airborne particles are concerns.

The mask uses a shingle pleat design. This design helps prevent fluid from pooling on the mask surface. It also helps reduce the potential for cross-contamination from pooled fluids.

Comfortable Earloop Design

The SafeMask Premier Elite Teal features soft, strong earloops. Medicom states that the earloops are ultrasonically sealed. They are attached to the outside of the mask. This design helps reduce pulling and irritation around the ears. It also supports easier mask removal with less risk of self-contamination.

An adjustable nosepiece provides a more personalized fit. The nosepiece helps the mask sit securely across the face. The mask also uses non-woven layers designed to resist linting, tearing, and shredding.

Teal SafeMask Premier Elite Features

The 2043 Teal model is listed by AccessGUDID as a surgical or medical face mask. It is classified as a non-antimicrobial, single-use device. The regulatory record identifies AMD Medicom Inc. as the manufacturer.

The mask is latex-free according to Medicom's product information. It is also supplied as a non-sterile disposable medical mask.

The standard configuration contains 50 masks per box. The official technical data identifies model 2043 as the Teal version. It lists 50 masks per box and 10 boxes per case.

Product Specifications : Medicom SafeMask Earloop Premier Elite Teal ASTM Level 3

• Brand: Medicom
• Product: SafeMask Premier Elite Earloop Mask
• Color: Teal
• ASTM Level: Level 3
• Model: 2043
• Design: Pleated earloop mask
• Nosepiece: Adjustable aluminum nosepiece
• Earloops: Ultrasonically sealed
• Sterility: Non-sterile
• Use: Single-use
• Latex: Latex-free
• Packaging: 50 masks per box; 500 masks per case

The Medicom SafeMask Earloop Premier Elite Teal combines high-barrier protection with a comfortable earloop design. Its ASTM Level 3 classification makes it suitable for appropriate higher-risk procedures. Always follow applicable workplace and clinical mask-use guidelines.

• Pfizer 0.9% Bacteriostatic Sodium Chloride Injection 10mL DIN 00037818
• Bacteriostatic Sodium Chloride Injection is supplied for its stated clinical application. Confirm the configuration, compatibility, and intended use before ordering.
• Product details
• • Product type: Sodium Chloride Injection
  • Manufacturer: Pfizer

Use according to the manufacturer's instructions and applicable procedure. Browse related Sodium Chloride Injection.

Pfizer Bacteriostatic Sodium Chloride Injection in Canada

Pfizer 0.9% Bacteriostatic Sodium Chloride Injection is a sterile solution for injection. Health Canada lists Pfizer Canada ULC as the manufacturer. The product is marketed under DIN 00037818.

The solution contains sodium chloride 9mg/mL, equivalent to 0.9% sodium chloride. Health Canada lists intramuscular, subcutaneous, and intravenous administration routes.

Pfizer describes bacteriostatic 0.9% Sodium Chloride Injection as a sterile, nonpyrogenic, isotonic solution. It contains water for injection and a bacteriostatic preservative. The preservative is benzyl alcohol.

This product is intended for parenteral use after adding medications that require dilution. It can also dissolve medications requiring an aqueous vehicle before injection.

Key Features

• • Pfizer Canada product
  • DIN: 00037818
  • 0.9% sodium chloride
  • Sodium chloride: 9mg/mL
  • 10mL vial format
  • Sterile solution
  • Nonpyrogenic solution
  • Isotonic formulation
  • Bacteriostatic preservative
  • Benzyl alcohol preservative
  • Multiple-dose container
  • Intended for parenteral medication preparation

Common Applications

Pfizer Bacteriostatic Sodium Chloride Injection 10mL is used as a diluent. It supports medications requiring dilution or dissolution before injection.

Health Canada lists the product for intramuscular, subcutaneous, and intravenous administration. Healthcare professionals should determine suitability based on the medication and clinical requirements.

The multiple-dose container allows repeated withdrawals when used according to applicable instructions. Pfizer specifies that the preparation is intended for parenteral use after appropriate medication addition.

Product Specifications

Specification	Details
Brand	Pfizer
Product	Bacteriostatic Sodium Chloride Injection USP
DIN	00037818
Concentration	0.9% / 9mg/mL
Volume	10mL
Dosage Form	Solution
Preservative	Benzyl alcohol
Container	Multiple-dose vial
Manufacturer	Pfizer Canada ULC
Routes Listed	IM, SC, IV

• The Pfizer 0.9% Bacteriostatic Sodium Chloride Injection 10mL is a pharmaceutical diluent for appropriate parenteral medication preparation. Always verify compatibility and follow the product monograph and professional clinical protocols before use. 

Qty-(20/BOX)3M 8210, N95 respirator is designed for use for particles such as those from grinding, sanding, sweeping, sawing, bagging, or other dusty operations. This respirator can also help reduce inhalation exposures to certain airborne biological particles (examples: mold, Bacillus anthracis, Mycobacterium tuberculosis), but cannot eliminate the risk of contracting infection, illness, or disease. Details NIOSH approved for at least 95 percent filtration efficiency against certain non-oil based particles Two-strap design with welded dual point attachment helps provide a secure seal Cushioning nose foam Lightweight construction promotes greater worker acceptance and may help increase wear time Lightweight construction promotes greater worker acceptance and may help increase wear time Advanced electrostatic media is designed for ease of breathing During the public health emergency of the COVID-19 pandemic, these standard N95 “industrial” respirators may be used by healthcare professionals according to the U.S. FDA’s Emergency Use Authorization (EUA). 3M™ Particulate Respirator 8210 is not cleared by the U.S. FDA as a surgical mask, a surgical mask and is not considered fluid-resistant, therefore a face shield must be worn during use. The respirator incorporates 3M’s proprietary technology with advanced electrostatically charged microfiber filter media designed for ease of breathing. This respirator is compatible with a variety of protective eyewear and hearing protection. This particulate respirator is NIOSH (National Institute for Occupational Safety and Health) approved for environments containing certain non-oil-based particles and provides at least 95 percent filter efficiency. Breathing hazardous particles can pose a risk to your health. NIOSH, a Federal government regulatory agency, has tested and approved the 3M Particulate Respirator 8210, which is designed to help reduce exposure to certain airborne particles. WARNING: These respirators help reduce exposures to certain airborne contaminants. Before use, the wearer must read and understand the User Instructions provided as a part of the product packaging. In the U.S., a written respiratory protection program must be implemented meeting all the requirements of OSHA 1910.134 including training, fit testing, and medical evaluation. In Canada, CSA standards Z94.4 requirements must be met and/or requirements of the applicable jurisdiction, as appropriate. Misuse may result in sickness or death. For proper use, see package instructions, supervisor,

• 3.5 Mil
• Vinyl powder-free
• Latex-free, hypoallergenic
• For single-use only
• 100 Gloves / Box
• Powder-free Exam Gloves
• Compliance standards: ASTM D5250
• Smooth Finish
• Non-Sterile
• Ambidextrous
• Available in Extra Small, Small, Medium, Large, or Extra Large