GUDID 40643169654325

CLIPS CL8903 RANEY 200

MEDTRONIC PS MEDICAL, INC.

Surgical clip applier, single-use Surgical clip applier, single-use Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip Scalp wound clip

• Primary Device ID: 40643169654325
• NIH Device Record Key: a99d2ab7-748d-4eee-8387-4d904e2911b8
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: CL8903
• Company DUNS: 089055867
• Company Name: MEDTRONIC PS MEDICAL, INC.
• Device Count: 200
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169654327 [Unit of Use]
GS1	40643169654325 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050044

FDA Product Code

• HBO: CLIP, SCALP

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-13

Devices Manufactured by MEDTRONIC PS MEDICAL, INC.

• 00763000406073 - Becker: 2024-04-08 EDMS 46128 BECKER II BLUE PT LN
• 00763000467340 - NA: 2024-03-11 KIT 46442 EDM LUMBAR DRN CLS TIP 5PK
• 00763000406042 - NA: 2024-03-05 ASSEMBLY 46422 EDM DRAINAGE
• 00763000406080 - NA: 2024-03-05 DRAIN 27302 EDM LUMBAR W/120 GRAD CH
• 00763000431259 - Becker: 2024-03-05 EDMS 46129 EURO BECKER II BLUE PT LN
• 00763000529307 - Becker: 2024-03-05 BECKER 27609 W/NEEDLESLESS INJ. SITE
• 00763000529369 - Becker: 2024-03-05 KIT 25068 EDM 46124 46126
• 00763000467357 - NA: 2024-03-05 KIT 46441 EDM LUMBAR DRAINAGE 5PK