Rhythmlink® 279-930-24TP
by Rhythmlink International, LLC
Rhythmlink® 279-930-24TP is a Class II device made by Rhythmlink International, LLC, listed in FDA GUDID since 4 Aug 2021 (UDI-DI 00816312025507), 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 | Number00816312025507 | Date4 Aug 2021 | StatusListed |
Official records
- AccessGUDID record 00816312025507
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Rhythmlink®
- Generic name
- Analytical non-scalp cutaneous lead
- Model / reference
- 279-930-24TP
- Primary DI / UDI-DI
- 00816312025507
- FDA product code
- JXE
- GMDN term
- Analytical non-scalp cutaneous lead
- Device class
- Class II
- Regulation number
- 882.1550
- GUDID distribution status
- In Commercial Distribution
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