Richmar 400-882
Richmar 400-882 is a Class II device made by Clearlake-Tech Inc., listed in FDA GUDID since 2 Aug 2023 (UDI-DI 00850030915603), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850030915603 | Date2 Aug 2023 | StatusListed |
Official records
- AccessGUDID record 00850030915603
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Richmar
- Generic name
- Transcutaneous electrical stimulation electrode, reusable
- Model / reference
- 400-882
- Primary DI / UDI-DI
- 00850030915603
- FDA product code
- GXY
- GMDN term
- Transcutaneous electrical stimulation electrode, reusable
- Device class
- Class II
- Regulation number
- 882.1320
- GUDID distribution status
- In Commercial Distribution
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