Vaginal Specula, Medium 4912
Vaginal Specula, Medium 4912 is a Class II device made by Dynarex Corp., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00616784491226), 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 | Number00616784491226 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00616784491226
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vaginal Specula, Medium
- Generic name
- Vaginal speculum, single-use
- Model / reference
- 4912
- Primary DI / UDI-DI
- 00616784491226
- FDA product code
- HIB
- GMDN term
- Vaginal speculum, single-use
- Device class
- Class II
- Regulation number
- 884.4530
- GUDID distribution status
- In Commercial Distribution
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