A. Titan Instruments 1251 ND
A. Titan Instruments 1251 ND is a Class I device made by A.Titan Instruments, listed in FDA GUDID since 10 Jan 2023 (UDI-DI 00841685102722), 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 | Number00841685102722 | Date10 Jan 2023 | StatusListed |
Official records
- AccessGUDID record 00841685102722
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- A. Titan Instruments
- Generic name
- Tooth extraction forceps
- Model / reference
- 1251 ND
- Primary DI / UDI-DI
- 00841685102722
- FDA product code
- EMG
- GMDN term
- Tooth extraction forceps
- Device class
- Class I
- Regulation number
- 872.4565
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Dry Heat Sterilization
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