Identity
- Trade Name
- Covidien FDA UDI
- Generic Name
- Electrode conductive medium FDA UDI
- Device Name
- Neurodiagnostic Electrode Paste FDA UDI
- Model / Reference
- 30806692 FDA UDI
- Description
- Neurodiagnostic Electrode Paste FDA UDI
Identifiers
- Catalog Number
- 30806692 FDA UDI
- Primary DI / UDI-DI
- 10884521643161 FDA UDI
- FDA Product Code
- GYB FDA UDI
- GMDN Term
- Electrode conductive medium FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1275 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
- Total Volume — 4 Fluid Ounce FDA UDI
Category: Electrode conductive medium
Covidien by Cardinalhealth — 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
- Cardinalhealth
Sources (1)
- FDA UDI 1a8419d8-6262-48f6-b409-e97a10dcb2ca 37 fields · synced Jun 6, 2026