624 - Certi-Gauze Bandage Compress - 4" - 1/Unit R211-008

GUDID 00766588110080

624 - Certi-Gauze Bandage Compress - 4" - 1/Unit

Certified Safety Manufacturing, Inc.

Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad Non-woven gauze pad

• Primary Device ID: 00766588110080
• NIH Device Record Key: 5e9adda2-eb12-46a1-ae63-9b67a50c8b5f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 624 - Certi-Gauze Bandage Compress - 4" - 1/Unit
• Version Model Number: R211-008
• Catalog Number: R211-008
• Company DUNS: 788460483
• Company Name: Certified Safety Manufacturing, 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: 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: false

Customer Support Contacts

• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00766588110080 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K945004

FDA Product Code

• EFQ: GAUZE/SPONGE, INTERNAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-04-04
• Device Publish Date: 2023-01-27

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• 00766588007571 - 10R - New Mexico Body Fluid - Refill: 2024-03-22 10R - New Mexico Body Fluid - Refill
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