CST Class B 21 BBP - FAC 3 Shelf Cabinet K625-287

GUDID 00766588252872

CST Class B 21 BBP - FAC 3 Shelf Cabinet

Certified Safety Manufacturing, Inc.

First aid kit, medicated

• Primary Device ID: 00766588252872
• NIH Device Record Key: 569da171-8ae5-4288-bfb5-ea0cc2d4c3ae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CST Class B 21 BBP - FAC 3 Shelf Cabinet
• Version Model Number: K625-287
• Catalog Number: K625-287
• 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
• Phone: +1(816)483-9090
• Email: Info@certifiedsafety.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00766588252872 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K940249

FDA Product Code

• LRR: First Aid Kit with drug

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-05-30
• Device Publish Date: 2025-05-22

Devices Manufactured by Certified Safety Manufacturing, Inc.

• 00766588120676 - RR - UP Facilities - 75V: 2025-12-23 RR - UP Facilities - 75V
• 00766588235721 - 608 - Adhesive Bandages Plastic 2"x 3" - 6/unit: 2025-12-23 608 - Adhesive Bandages Plastic 2"x 3" - 6/unit
• 00766588160825 - 816 - Nitrile Gloves - 2 pr/unit: 2025-12-16 816 - Nitrile Gloves - 2 pr/unit
• 00766588190051 - QF Tape 1/2" x 2.5 yds. - Roll: 2025-12-16 QF Tape 1/2" x 2.5 yds. - Roll
• 00766588250083 - Safety General Purpose - 16 Poly White: 2025-12-16 Safety General Purpose - 16 Poly White
• 00766588069012 - Gillig Bus 24 - Refill: 2025-12-10 Gillig Bus 24 - Refill
• 00766588042053 - New Mexico SBK - 24 Poly White: 2025-08-29 New Mexico SBK - 24 Poly White
• 00766588089560 - Mississippi BFK - Refill: 2025-08-29 Mississippi BFK - Refill