Identity
- Trade Name
- Therabody FDA UDI
- Generic Name
- Electrode conductive medium FDA UDI
- Device Name
- TheraFace Conductive Gel Intended to be used with external electrodes to reduce the impedance of the contact between the electrode surface and the skin. FDA UDI
- Model / Reference
- TheraFace Conductive Gel FDA UDI
- Description
- TheraFace Conductive Gel Intended to be used with external electrodes to reduce the impedance of the contact between the electrode surface and the skin. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840295408224 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
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrode conductive medium
Therabody by Therabody, 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
- Therabody, Inc.
Sources (1)
- FDA UDI dc9cfdee-9da9-44cd-889c-7098899b5190 33 fields · synced May 30, 2026