Explorer
by Lifewatch
Explorer is a Class II device made by Lifewatch, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00850725007064), registry data as of 8 Jun 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850725007064 | Date16 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00850725007064
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Electrocardiography telemetric monitoring system transmitter
- Model / reference
- Explorer
- Description
- Card Guard Personal Electrocardiogram Transmitter
- Primary DI / UDI-DI
- 00850725007064
- FDA product code
- DXH
- GMDN term
- Electrocardiography telemetric monitoring system transmitter
- Device class
- Class II
- Regulation number
- 870.2920
- GUDID distribution status
- In Commercial Distribution
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