Henry Schein 1000001
Henry Schein 1000001 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 26 Nov 2019 (UDI-DI 00304040043516), 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 | Number00304040043516 | Date26 Nov 2019 | StatusListed |
Official records
- AccessGUDID record 00304040043516
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Henry Schein
- Generic name
- Tooth extraction forceps
- Model / Ref / Catalog
- 1000001
- Primary DI / UDI-DI
- 00304040043516
- 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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