PowerDot PD-01MB
PowerDot PD-01MB is a Class II device made by ZMI Electronics Ltd., listed in FDA GUDID since 12 Feb 2018 (UDI-DI 04719872330387), 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 | Number04719872330387 | Date12 Feb 2018 | StatusListed |
Official records
- AccessGUDID record 04719872330387
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PowerDot
- Generic name
- Multi-modality physical therapy system, simultaneous, professional-use
- Model / Ref / Catalog
- PD-01MB, PD-01M
- Primary DI / UDI-DI
- 04719872330387
- FDA product code
- NGX
- GMDN term
- Multi-modality physical therapy system, simultaneous, professional-use
- Device class
- Class II
- Regulation number
- 890.5850
- GUDID distribution status
- In Commercial Distribution
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