Patient Armor Ear Loop Masks AM2200B

GUDID 00858653006173

Patient Armor- Earloop Mask Fluid Resistant (BLUE) -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: 00858653006173
• NIH Device Record Key: b23d4460-648a-4524-862d-86c9e3416c3b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Patient Armor Ear Loop Masks
• Version Model Number: Blue
• Catalog Number: AM2200B
• 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	00858653006173 [Primary]
GS1	10858653006170 [Package]; Package: Case [10 Units]; In Commercial Distribution

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: 2016-05-12

On-Brand Devices [Patient Armor Ear Loop Masks]

• 00858653006197: Patient Armor- Earloop Mask Fluid Resistant (PINK) -50/Bx.
• 00858653006180: Patient Armor- Earloop Mask Fluid Resistant (ORCHID) - 50/Bx
• 00858653006173: Patient Armor- Earloop Mask Fluid Resistant (BLUE) -50/Bx.