Identity
- Trade Name
- Nalu Medical, Inc. FDA UDI
- Generic Name
- Analgesic implantable peripheral nerve electrical stimulation system FDA UDI
- Device Name
- Nalu Neurostimulation Kit (Ported, Single 4) FDA UDI
- Model / Reference
- 71007-US FDA UDI
- Description
- Nalu Neurostimulation Kit (Ported, Single 4) FDA UDI
Identifiers
- Catalog Number
- 71007-US FDA UDI
- Primary DI / UDI-DI
- 00812537035512 FDA UDI
- FDA Product Code
- GZF FDA UDI
- GMDN Term
- Analgesic implantable peripheral nerve electrical stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5870 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
Category: Analgesic implantable peripheral nerve electrical stimulation system
Nalu Medical, Inc. by Nalu Medical — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Nalu Medical
Sources (1)
- FDA UDI 0e4c5ad6-8f11-4c3c-995c-e517b6c104db 36 fields · synced Jun 1, 2026