Identity
- Trade Name
- TELIGEN FDA UDI
- Generic Name
- Nerve-locating system probe, single-use FDA UDI
- Device Name
- TELIGEN ACCESS PROBE FDA UDI
- Model / Reference
- 286006062S FDA UDI
- Description
- TELIGEN ACCESS PROBE FDA UDI
Identifiers
- Catalog Number
- 286006062S FDA UDI
- Primary DI / UDI-DI
- 10705034604527 FDA UDI
- FDA Product Code
- OLO FDA UDIPDQ FDA UDI
- GMDN Term
- Nerve-locating system probe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI874.1820 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Nerve-locating system probe, single-use
Teligen by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nerve-locating system probe, single-use.
- Cadwell — Technomed Engineering B.V. · Class II
- ALARA Neuro Access Needle Kit — SURGENTEC LLC · Class II
- Nerve Stimulator Probe — Koros USA, Inc. · Class II
- Dragonfly® — NEUROVISION MEDICAL PRODUCTS, INC. · Class II
- Cobra® — NEUROVISION MEDICAL PRODUCTS, INC. · Class II
- SafeOp 3 — ALPHATEC SPINE, INC. · Class II
- IOM Stimulator Probes — SPES MEDICA SPA · Class II
- NIM-Spine® — MEDTRONIC SOFAMOR DANEK, INC. · Class II
Cleared under the same submission
K223108 also covers:
K223438 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (1)
- FDA UDI 346c750c-ad5b-4341-8c5d-3e69de3b4ee4 36 fields · synced May 29, 2026