Identity
- Trade Name
- Prospera FDA UDI
- Generic Name
- Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator FDA UDI
- Model / Reference
- EPG FDA UDI
Identifiers
- Catalog Number
- 457861 FDA UDI
- Primary DI / UDI-DI
- 04035479170127 FDA UDI
- PMA Number
- P210037 FDA UDI
- FDA Product Code
- LGW FDA UDI
- GMDN Term
- Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator FDA UDI
Classification
- Device Class
- Class III 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
Prospera by BIOTRONIK SE & Co. KG — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
P210037 also covers:
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- BIOTRONIK — BIOTRONIK SE & Co. KG
- Neuro CP app 2300.U — BIOTRONIK SE & Co. KG
- Neuro PR app 2400.U — BIOTRONIK SE & Co. KG
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
- BIOTRONIK SE & Co. KG
Sources (1)
- FDA UDI e5341d99-8ce9-4851-80e8-f808e296eb2d 36 fields · synced May 30, 2026