GUDID 00885074200224

ACCY KIT 355038 TUNNELING TL 1X8 38CM ID

MEDTRONIC, INC.

Subcutaneous tunneller, single-use

• Primary Device ID: 00885074200224
• NIH Device Record Key: c4c71637-ac3c-4706-a219-537ad98a2fbe
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 355038
• Company DUNS: 796986144
• Company Name: MEDTRONIC, 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885074200224 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P840001

FDA Product Code

• LGW: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

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: 2014-09-23

Devices Manufactured by MEDTRONIC, INC.

• 00199150039371 - NA: 2025-08-22 CUSTOM PACK BB11U72R1 P/T
• 00199150040872 - NA: 2025-08-22 CUSTOM PACK BB4K95R22 HLO PERFNPLEG
• 00199150041145 - NA: 2025-08-22 CUSTOM PACK BB12Q87R1 HLN VAMC NASH
• 00199150041978 - NA: 2025-08-22 CUSTOM PACK BB10F40R2 ACCESORY
• 00199150041299 - NA: 2025-08-19 CUSTOM PACK BB8E60R12 EVL PED E
• 20199150041118 - NA: 2025-08-18 CUSTOM PACK BB12E30R1 10PK ACC BRIDGE
• 20199150041132 - NA: 2025-08-18 CUSTOM PACK BB5G89R2 2PK T SPRT
• 00763000876982 - SPRINTER® LEGEND: 2025-08-18 BALLOON SPL12506X SPR LEG RX US M