Pe-Fo
Pe-Fo (302-10004) is a Class I device made by Quality Aspirators, listed in FDA GUDID since 27 Feb 2025 (UDI-DI 00814005023489), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00814005023489 | Date27 Feb 2025 | StatusListed |
Official records
- AccessGUDID record 00814005023489
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- General-purpose light source
- Model / Ref / Catalog
- PE-FO, 302-10004
- Primary DI / UDI-DI
- 00814005023489
- FDA product code
- EAY
- GMDN term
- General-purpose light source
- Device class
- Class I
- Regulation number
- 872.4620
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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