Identity
- Trade Name
- N'VISION® FDA UDI
- Generic Name
- Multiple active implantable device programmer FDA UDI
- Device Name
- SFTWR 8870MMB US MKT MMB/02 BOWEL FDA UDI
- Model / Reference
- 8870MMB02 FDA UDI
- Description
- SFTWR 8870MMB US MKT MMB/02 BOWEL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00613994606846 FDA UDI
- PMA Number
- P970004 FDA UDI
- FDA Product Code
- LNQ FDA UDIEZW FDA UDIQON FDA UDI
- GMDN Term
- Multiple active implantable device programmer FDA UDI
Classification
- Device Class
- Unclassified FDA UDI
- Regulation Number
- 876.5270 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multiple active implantable device programmer
N'vision® by Medtronic, Inc. — Class Unclassified — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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® II — MEDTRONIC, INC.
- InterStim iCon — MEDTRONIC, INC.
- InterStim™ — 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 Unclassified | Pending data |
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Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI 71faed12-5e92-4f6b-9b27-f9116643f61b 36 fields · synced May 30, 2026