Bloodborne Pathogen Kit - 19 Piece S-16500

GUDID 10851253007660

"(1) ABSORBENT POWDER (4) ANTISEPTIC TOWELETTE (1) BAG WITH SCOOP (1) BIOHAZARD BAG (1) BOUFFANT CAP (1) CPROTECTOR (1) GOWN (3) INSTANT HAND SANITIZER (2) NITRILE GLOVE 2 (2) PAPER TOWEL (2) GERMICIDAL WIPE (1) DISPOSABLE FACE MASK WITH SHIELD"

ULINE, INC.

Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use Cardiopulmonary resuscitation mask, single-use

• Primary Device ID: 10851253007660
• NIH Device Record Key: 90a4f562-5704-4d9c-9887-7ffb490cb3aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bloodborne Pathogen Kit - 19 Piece
• Version Model Number: S-16500
• Catalog Number: S-16500
• Company DUNS: 039612668
• Company Name: ULINE, 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: true
• Device Combination Product: true
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	10851253007660 [Primary]

FDA Product Code

• CBP: Valve, Non-Rebreathing

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: 2022-01-10
• Device Publish Date: 2019-02-22

On-Brand Devices [Bloodborne Pathogen Kit - 19 Piece]

• 10851253007660: "(1) ABSORBENT POWDER (4) ANTISEPTIC TOWELETTE (1) BAG WITH SCOOP (1) BIOHAZARD BAG (1) BOUFFANT
• 10850015055352: (1) ABSORBENT POWDER (4) ANTISEPTIC TOWELETTE (1) PLASTIC SCOOP (1) BIOHAZARD BAG 10 GALLON WITH