Henry Schein 9004526
Ref 9004526Model TF-010
Henry Schein 9004526 is a carbide dental bur (EU MDD Class IIa; FDA Class I; FDA product code EJL, Bur, Dental) made by Henry Schein, Inc., registered in EUDAMED on 28 May 2026 (Basic UDI-DI B-10304040075828) and listed in FDA GUDID since 12 Nov 2019 (UDI-DI 10304040075828), active as of 23 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-10304040075828 10304040075828 | Date28 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10304040075828 | Date12 Nov 2019 | StatusListed |
Official records
- EUDAMED public site B-10304040075828
- AccessGUDID record 00304040075821
Across registries
- EUDAMED Basic UDI-DI B-10304040075828 registered 28 May 2026 Active
- FDA GUDID UDI-DI 10304040075828 listed 12 Nov 2019 Listed
Timeline
- Listed FDA GUDID 10304040075828
- Registered EUDAMED B-10304040075828
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Henry Schein Maxima EUDAMEDHenry Schein GUDID
- Generic name
- Carbide dental bur, reusable
- Device name
- Steel & TC Burs
- Model / Ref / Catalog
- 9004526, TF-010
- Primary DI / UDI-DI
- 10304040075828 EUDAMED00304040075821 GUDID
- Basic UDI-DI
- B-10304040075828
- FDA product code
- EJL
- EMDN code
- Z12110102 Dental drills
- GMDN term
- Carbide dental bur, reusable
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 872.3240
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Primary DI / UDI-DI | 10304040075828 | 00304040075821 |
| Device class | Class IIa | Class I |
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