Identity
- Trade Name
- Alpine BioMed FDA UDI
- Generic Name
- Nerve-locating system FDA UDI
- Device Name
- CLAVIS, DEVICE COMPLETE FDA UDI
- Model / Reference
- 9015A0012JP FDA UDI
- Description
- CLAVIS, DEVICE COMPLETE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05704736009546 FDA UDI
- 510(k) Number
- K062478 FDA UDI
- FDA Product Code
- GWL FDA UDIBXN FDA UDI
- GMDN Term
- Nerve-locating system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1835 FDA UDI868.2775 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Alpine BioMed by Alpine Biomed Aps — 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
- Alpine Biomed Aps
Sources (1)
- FDA UDI 74f44333-0c0f-4cfa-b765-60915a7a7828 35 fields · synced Jun 8, 2026