Delice - Chéri - Kegel Trainer - Purple
Delice - Chéri - Kegel Trainer - Purple (BL-23721) is a Class II device made by Blush Novelties, listed in FDA GUDID since 13 Mar 2025 (UDI-DI 00810138370834), 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 | Number00810138370834 | Date13 Mar 2025 | StatusListed |
Official records
- AccessGUDID record 00810138370834
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Delice
- Generic name
- Perineometer
- Model / Ref / Catalog
- Delice - Chéri - Kegel Trainer - Purple, BL-23721
- Primary DI / UDI-DI
- 00810138370834
- FDA product code
- HIR
- GMDN term
- Perineometer
- Device class
- Class II
- Regulation number
- 884.1425
- GUDID distribution status
- In Commercial Distribution
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