Breeze 33990901
Breeze 33990901 is a Class I device made by Dolgencorp, LLC, listed in FDA GUDID since 17 Jan 2023 (UDI-DI 00090891949670), 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 | Number00090891949670 | Date17 Jan 2023 | StatusListed |
Official records
- AccessGUDID record 00090891949670
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Breeze
- Generic name
- Menstrual pad, unscented
- Model / reference
- 33990901
- Primary DI / UDI-DI
- 00090891949670
- FDA product code
- HHD
- GMDN term
- Menstrual pad, unscented
- Device class
- Class I
- Regulation number
- 884.5435
- GUDID distribution status
- In Commercial Distribution
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