Identity
- Trade Name
- C.M.P. Cable FDA UDI
- Generic Name
- Transcutaneous electrical stimulation lead FDA UDI
- Device Name
- Single 0.080" Socket to 0.080" Pin Wire Extender 72" lead wire FDA UDI
- Model / Reference
- W9672 FDA UDI
- Description
- Single 0.080" Socket to 0.080" Pin Wire Extender 72" lead wire FDA UDI
Identifiers
- Primary DI / UDI-DI
- B312W96720 FDA UDI
- FDA Product Code
- IKD FDA UDI
- GMDN Term
- Transcutaneous electrical stimulation lead FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.1175 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
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Transcutaneous electrical stimulation lead
C.M.P. Cable by C.M.P. Canadian Medical Products Inc — 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
- C.M.P. Canadian Medical Products Inc
Sources (1)
- FDA UDI cd384264-1f66-4dd2-8956-882d38dd1641 33 fields · synced May 30, 2026