Biotricity 1.0
Biotricity 1.0 is a Class II device made by Biotricity, Inc., listed in FDA GUDID since 17 Feb 2022 (UDI-DI B635BIOTRES100), 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 | NumberB635BIOTRES100 | Date17 Feb 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Biotricity
- Generic name
- Electrocardiography telemetric monitoring system transmitter
- Model / reference
- 1.0
- Primary DI / UDI-DI
- B635BIOTRES100
- FDA product code
- MWJ
- GMDN term
- Electrocardiography telemetric monitoring system transmitter
- Device class
- Class II
- Regulation number
- 870.2800
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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