A.C.E Blue PD9505
A.C.E Blue PD9505 is a Class II device made by Pulsaderm LLC, listed in FDA GUDID since 4 Oct 2018 (UDI-DI 00864918000305), registry data as of 22 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 | Number00864918000305 | Date4 Oct 2018 | StatusListed |
Official records
- AccessGUDID record 00864918000305
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- A.C.E Blue
- Generic name
- Red/blue light phototherapy unit
- Model / reference
- PD9505
- Primary DI / UDI-DI
- 00864918000305
- FDA product code
- OLP
- GMDN term
- Red/blue light phototherapy unit
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
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