Identity
- Trade Name
- MENIETT® FDA UDI
- Generic Name
- Primary battery FDA UDI
- Device Name
- BATTERY 1010021005 MENIETT 9.6VDC ROHS FDA UDI
- Model / Reference
- 1010021005 FDA UDI
- Description
- BATTERY 1010021005 MENIETT 9.6VDC ROHS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00721902326257 FDA UDI
- FDA Product Code
- ETY FDA UDI
- GMDN Term
- Primary battery FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.1090 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Meniett® by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Xomed, Inc.
Sources (1)
- FDA UDI 97235e32-387b-4dfd-8254-e9a46395be91 35 fields · synced May 30, 2026