Patient Armor Ear Loop Masks ASTM Level 2 PA002L

GUDID 00858653006272

Fluid Resistant Earloop Mask ASTM Level 2 (Lavender) - 50/Bx

AMERICAN MEDICAL & HOSPITAL SUPPLY CO., INC.

Surgical/medical respirator, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use Surgical/medical respirator, non-antimicrobial, single-use

• Primary Device ID: 00858653006272
• NIH Device Record Key: 0e2dc489-d101-4486-874a-c4ee8c570748
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Patient Armor Ear Loop Masks ASTM Level 2
• Version Model Number: Lavender
• Catalog Number: PA002L
• Company DUNS: 180611519
• Company Name: AMERICAN MEDICAL & HOSPITAL SUPPLY CO., INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00858653006272 [Primary]

FDA Product Code

• FXX: Mask, Surgical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-05-06
• Device Publish Date: 2018-02-01

On-Brand Devices [Patient Armor Ear Loop Masks ASTM Level 2]

• 00858653006302: Fluid Resistant Earloop Mask ASTM Level 2 (White) - 50/Bx
• 00858653006296: Fluid Resistant Earloop Mask ASTM Level 2 (Pink) - 50/Bx
• 00858653006289: Fluid Resistant Earloop Mask ASTM Level 2 (Blue) - 50/Bx
• 00858653006272: Fluid Resistant Earloop Mask ASTM Level 2 (Lavender) - 50/Bx