Identity
- Trade Name
- Algovita® FDA UDI
- Generic Name
- Analgesic spinal cord electrical stimulation system FDA UDI
- Device Name
- Algovita® 12 Electrode Percutaneous Lead Kit - (compact). Electrode spacing 1 mm FDA UDI
- Model / Reference
- 1121-45-USA FDA UDI
- Description
- Algovita® 12 Electrode Percutaneous Lead Kit - (compact). Electrode spacing 1 mm FDA UDI
Identifiers
- Catalog Number
- 1121-45 FDA UDI
- Primary DI / UDI-DI
- 00821329580147 FDA UDI
- FDA Product Code
- LGW FDA UDI
- GMDN Term
- Analgesic spinal cord electrical stimulation system FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 45 Centimeter FDA UDI
Category: Analgesic spinal cord electrical stimulation system
Algovita® by Greatbatch Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Greatbatch Ltd
Sources (1)
- FDA UDI 951ab945-5a39-485a-bfb5-35743651cf33 36 fields · synced May 30, 2026