GUDID 00643169466548

AD 22039 12MM

MEDTRONIC PS MEDICAL, INC.

Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir Cranial port/reservoir

• Primary Device ID: 00643169466548
• NIH Device Record Key: eabdda64-3613-43bc-9acb-ea2ff1e3408a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 22039
• Company DUNS: 089055867
• Company Name: MEDTRONIC PS MEDICAL, 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169466548 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K833822

FDA Product Code

• JXG: Shunt, central nervous system and components

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-03-05
• Device Publish Date: 2015-07-10

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