Mediblu HA3P
Mediblu HA3P (MDB01023) is a Class II device made by Mediblu Medical, LLC, listed in FDA GUDID since 25 Jun 2020 (UDI-DI B632MDB01023), 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 | NumberB632MDB01023 | Date25 Jun 2020 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mediblu
- Generic name
- Electrocardiographic ambulatory recorder
- Model / Ref / Catalog
- HA3P, MDB01023
- Primary DI / UDI-DI
- B632MDB01023
- FDA product code
- MWJ
- GMDN term
- Electrocardiographic ambulatory recorder
- Device class
- Class II
- Regulation number
- 870.2800
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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