Kohdent 1302
by Kohler Medizintechnik GmbH & Co. KG
Kohdent 1302 is a Class I device made by Kohler Medizintechnik GmbH & Co. KG, listed in FDA GUDID since 30 Aug 2021 (UDI-DI 04251436901942), 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 | Number04251436901942 | Date30 Aug 2021 | StatusListed |
Official records
- AccessGUDID record 04251436901942
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Kohdent
- Generic name
- Tooth extraction forceps
- Model / Ref / Catalog
- 1302
- Primary DI / UDI-DI
- 04251436901942
- 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
- Moist Heat or Steam Sterilization
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