LOLA Trial Set
by Alyk, Inc.
LOLA Trial Set is a Class II device made by Alyk, Inc., listed in FDA GUDID since 5 Dec 2019 (UDI-DI 00851617007131), 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 | Number00851617007131 | Date5 Dec 2019 | StatusListed |
Official records
- AccessGUDID record 00851617007131
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Lola
- Generic name
- Menstrual tampon, unscented
- Model / reference
- Trial Set
- Primary DI / UDI-DI
- 00851617007131
- FDA product code
- HEB
- GMDN term
- Menstrual tampon, unscented
- Device class
- Class II
- Regulation number
- 884.5470
- GUDID distribution status
- In Commercial Distribution
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