Ventlab BR303
Ventlab BR303 is an atomizer (FDA Class II; FDA product code CAF, Nebulizer (Direct Patient Interface)) made by Ventlab Corp., listed in FDA GUDID since 30 Sep 2016 (UDI-DI 10889483091036), 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 | Number10889483091036 | Date30 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10889483091036
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ventlab
- Generic name
- Atomizer, non-ventilatory
- Model / reference
- BR303
- Primary DI / UDI-DI
- 10889483091036
- FDA product code
- CAF
- GMDN term
- Atomizer, non-ventilatory
- Device class
- Class II
- Regulation number
- 868.5630
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 22 Millimeter
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Other devices filed under FDA product code CAF (Nebulizer (Direct Patient Interface)).
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