LifeSignals LP1251
LifeSignals LP1251 (LP1251_US) is a Class II device made by LifeSignals, Inc., listed in FDA GUDID since 15 Nov 2021 (UDI-DI B353LP12511), registry data as of 23 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 | NumberB353LP12511 | Date15 Nov 2021 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- LifeSignals
- Generic name
- Electrocardiographic ambulatory recorder
- Model / Ref / Catalog
- LP1251, LP1251_US
- Primary DI / UDI-DI
- B353LP12511
- FDA product code
- DRG, MWJ
- GMDN term
- Electrocardiographic ambulatory recorder
- Device class
- Class II
- Regulation number
- 870.2910, 870.2800
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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