Identity
- Trade Name
- InterStim™ FDA UDI
- Generic Name
- Neurosurgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- ACCY 041826 INTRSTIM GROUND PAD GLBL MDR FDA UDI
- Model / Reference
- 041826 FDA UDI
- Description
- ACCY 041826 INTRSTIM GROUND PAD GLBL MDR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20763000343273 FDA UDI
- FDA Product Code
- EZW FDA UDI
- GMDN Term
- Neurosurgical procedure kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 876.5270 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Neurosurgical procedure kit, non-medicated, single-use
InterStim™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Neurosurgical procedure kit, non-medicated, single-use.
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
Cleared under the same submission
P080025 also covers:
- INTERSTIM — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® II — MEDTRONIC, INC.
- INTERSTIM® Twist-Lock Cable — MEDTRONIC, INC.
- InterStim™ — MEDTRONIC, INC.
- InterStim™ — MEDTRONIC, INC.
- InterStim™ — MEDTRONIC, INC.
P970004 also covers:
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® — MEDTRONIC, INC.
- INTERSTIM® II — MEDTRONIC, INC.
- InterStim iCon — MEDTRONIC, INC.
- InterStim™ — MEDTRONIC, INC.
- InterStim™ — MEDTRONIC, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI 23e4ea10-43ad-4a4e-9dc7-9f049f353fa8 35 fields · synced May 30, 2026