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GTDI item MR-1101

Procedure mask, ear loop, fiberglass-free filter, blue

  • Not made with natural rubber latex

Pleated polypropylene procedure mask with elastic ear loops, a flexible nose piece and a fiberglass-free filter, blue. Bacterial filtration efficiency 98% or higher as stated by the manufacturer, which states no ASTM F2100 level and lists the mask as not fluid resistant. Not made with natural rubber latex; DEHP-free as stated. Made in China. 50 masks per box, 12 boxes per case.

50 per box, 12 boxes Face masks
Render of an ear-loop procedure mask
Illustration of the product type. The manufacturer and brand are named on your written quote.

Specifications

Attribute, value and basisValues as stated by the manufacturer. The standard or test behind each value is named in the row.
Attribute Value Basis
Identity and regulatory status
GTDI item code MR-1101 Internal
Material and construction
Filter Fiberglass-free, as stated by the manufacturer Manufacturer specification
Material Polypropylene (PP) Manufacturer specification
Style Pleated Manufacturer specification
Fastening Elastic ear loops Manufacturer specification
Nose piece Flexible nose piece Manufacturer specification
Color Blue Manufacturer specification
Performance, testing and labeling
Fluid resistant No Manufacturer specification
Bacterial filtration efficiency 98% or higher, as stated by the manufacturer Manufacturer specification
Natural rubber latex Not made with natural rubber latex, as stated by the manufacturer Manufacturer specification
DEHP DEHP-free, as stated by the manufacturer Manufacturer specification
Storage, origin and packaging
Country of origin China Manufacturer specification
Packaging 50 masks per box, 12 boxes per case Manufacturer specification

Sizes and packaging

Pack-out by size
Size or variant Variant code Masks per pack Packs per case Masks per case
Blue, 50 per box MR-1101-EA 50 12 600

Standards, testing and claims

Not made with natural rubber latex
Basis: Manufacturer labeling; FDA labeling guidance
Manufacturer statement
Bacterial filtration efficiency 98% or higher, as stated by the manufacturer.Basis: As stated by the manufacturer; the document is supplied with the quote

Provided with your quote

  • Brochure Supplied with your written quote, before you order With the quote
  • Document Supplied with your written quote, before you order With the quote

We substitute only with your written approval. A change of manufacturer counts as a substitution.

Compare with other procedure and surgical masks

Procedure and surgical masksValues as each product page states them. An empty cell means the manufacturer states no value.
Product ASTM level Attachment Layers Features Color Per box
Procedure mask, ear loop, blueGTDI item MR-1101, this page Elastic ear loops Blue 50
ASTM Level 1 procedure mask, ear loopGTDI item MR-1102 Level 1 Soft ear loops No Blue 50
ASTM Level 1 procedure mask, 3-plyGTDI item MR-1103 Level 1 Elastic ear loops 3-ply Blue 50
ASTM Level 3 surgical mask, tie-onGTDI item MR-1104 Level 3 Ties Anti-glare eye shield Orange 25
ASTM Level 3 procedure mask, ear loopGTDI item MR-1105 Level 3 Ear loops 4-ply Built-in foam anti-fog strip Violet 50

All procedure and surgical masks

Questions buyers ask about masks and respirators

  • Compare the test figures, not the mask's color or name.
  • Masks with an attached eye shield come 25 per box. Most others come 50.
Do we need a fluid barrier or airborne protection?

A mask protects against splashes and large droplets and is an FDA device under 21 CFR 878.4040. A respirator filters airborne particles and is approved by NIOSH under 42 CFR part 84. The task decides which, and the two are never interchangeable.

Which ASTM level suits which task?

ASTM F2100 rates masks at Level 1, 2 or 3 on bacterial and particulate filtration, breathability and resistance to synthetic blood at 80, 120 or 160 mmHg. Higher fluid resistance suits procedures with splash risk. Each listing shows the level and the test values behind it, as the edition on the manufacturer's test report states them.

Is this respirator NIOSH Approved, and how do we check?

Every respirator listed as N95 holds a current NIOSH approval. The TC approval number is on your quote so you can confirm it on the NIOSH Certified Equipment List. NIOSH treats "N95" and "NIOSH Approved" as registered certification marks, and a product without an approval may not carry them.

Surgical N95 or standard N95?

A surgical N95 is a NIOSH Approved respirator that is also fluid resistant and regulated by FDA as a Class II device. It is unvalved and states its fluid resistance level. A standard N95 is NIOSH Approved only. Sterile fields and procedure rooms call for the surgical version.

Is this the model our staff are fit-tested to?

Fit testing applies to the make, model, style and size tested. Tell us the model your staff are fit-tested to. Your quote confirms that exact model or names an alternative for your approval, and nothing is substituted without it.

What is the shelf life, and how do we rotate a stockpile?

Manufacturers set a shelf life, often about five years. Past its shelf life a respirator is no longer NIOSH Approved. Each listing shows the shelf life as stated, and quotes state the dating at shipment, so a stockpile can be rotated by date.

When is a KN95 acceptable?

A KN95 is made to China's GB 2626 standard and is not NIOSH Approved. It is listed plainly as such and is not for use where a NIOSH Approved respirator is required.

Talk to the accounts team.

Phone, email and address are the same on every page of this site, on every quote and on every invoice.

  • Phone 424-832-6485
  • Email sales@gtdi.net
  • Hours Monday to Friday, 8 a.m. to 5 p.m. Pacific
  • Address GTDI, 200 S Barrington Ave, Los Angeles, CA 90049

Your first contact is the GTDI accounts team. Existing accounts: your representative's direct contact is on your account dashboard.