Identity
- Trade Name
- Uni-Patch FDA UDI
- Generic Name
- Electrode conductive skin pad, single-use FDA UDI
- Device Name
- Carbon Electrode Tape Patch,125C-LT, Cloth, Low Tack, Slit Opening FDA UDI
- Model / Reference
- MT70000 FDA UDI
- Description
- Carbon Electrode Tape Patch,125C-LT, Cloth, Low Tack, Slit Opening FDA UDI
Identifiers
- Catalog Number
- MT70000 FDA UDI
- Primary DI / UDI-DI
- 20884527021335 FDA UDI
- FDA Product Code
- KGX FDA UDI
- GMDN Term
- Electrode conductive skin pad, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5240 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Dimensions & Sizes
- Size
- Width — 3 Inch FDA UDILength — 3 Inch FDA UDI
Uni-Patch by Cardinalhealth — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cardinalhealth
Sources (1)
- FDA UDI 74988108-43e0-459f-90f6-f632c0eb8874 37 fields · synced May 30, 2026