ProTrap Luma BBPA10001
ProTrap Luma BBPA10001 is a Class II device made by Micro-tech Usa, listed in FDA GUDID since 3 Mar 2025 (UDI-DI 00858276007946), 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 | Number00858276007946 | Date3 Mar 2025 | StatusListed |
Official records
- AccessGUDID record 00858276007946
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- ProTrap Luma
- Generic name
- Surgical suction system collection container, single-use
- Model / reference
- BBPA10001
- Primary DI / UDI-DI
- 00858276007946
- FDA product code
- KDQ
- GMDN term
- Surgical suction system collection container, single-use
- Device class
- Class II
- Regulation number
- 880.6740
- GUDID distribution status
- In Commercial Distribution
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