Identity
- Trade Name
- Cadwell Replacement Stimulator Probe FDA UDI
- Generic Name
- Nerve-locating system probe, reusable FDA UDI
- Model / Reference
- 339084-200 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840067102107 FDA UDI
- FDA Product Code
- GWF FDA UDI
- GMDN Term
- Nerve-locating system probe, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1870 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 0.31 Inch FDA UDI
Category: Nerve-locating system probe, reusable
Cadwell Replacement Stimulator Probe by Cadwell Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Nerve-locating system probe, reusable.
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- Cadwell Replacement Stimulator Probe — Cadwell Industries, Inc. · Class II
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
- Cadwell Industries, Inc.
Sources (1)
- FDA UDI 87c52019-c367-4cb2-91ed-fbb28f90aaa0 34 fields · synced Jun 9, 2026