Dilator 32-430-08-01
Dilator 32-430-08-01 is a Class I device made by KLS-Martin L.P., listed in FDA GUDID since 26 Sep 2018 (UDI-DI 00888118055262), 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 | Number00888118055262 | Date26 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 00888118055262
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dilator
- Generic name
- Vaginal dilator
- Model / reference
- 32-430-08-01
- Primary DI / UDI-DI
- 00888118055262
- FDA product code
- HDQ
- GMDN term
- Vaginal dilator
- Device class
- Class I
- Regulation number
- 884.4530
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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