← Back to catalogue
HM Bohrer FGL - konisch
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref H23L.314.009Model 10521Ref H23.314.016
Identity
- Trade Name
- HM Bohrer FGL - konisch EUDAMEDEDENTA FDA UDI
- Generic Name
- Carbide dental bur, reusable FDA UDI
- Device Name
- HM-/Stahl-Bohrer EUDAMEDTC Bur FGL - tapered FDA UDI
- Model / Reference
- 10521 EUDAMEDH23L.314.009 EUDAMEDFDA UDIH23.314.016 EUDAMED
- Description
- TC Bur FGL - tapered FDA UDI
Identifiers
- Catalog Number
- H169L-FG FDA UDI
- Primary DI / UDI-DI
- E312H23L3140091 EUDAMEDFDA UDIE312H233140161 EUDAMED
- Basic UDI-DI
- ++E31210521CQ EUDAMED
- Unit of Use DI
- E312H23L314009101 EUDAMEDE312H23314016101 EUDAMED
- FDA Product Code
- EJL FDA UDI
- EMDN Code
- L159007 ODONTOSTOMATOLOGY BURS, REUSABLE EUDAMED
- GMDN Term
- Carbide dental bur, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.3240 FDA UDI
- Market of Registration
- Liechtenstein EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
HM Bohrer FGL - konisch by Edenta Etablissement — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++E31210521CQ | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Edenta Etablissement
- EUDAMED SRN
- LI-MF-000011937
Sources (3)
- EUDAMED 52e6bcc9-1ed0-4f4c-bc2b-dde20fabc721 61 fields · synced Jul 29, 2026
- EUDAMED fa18486f-825f-4951-ba77-848d1ff10d91 61 fields · synced May 17, 2026
- FDA UDI 96e4887d-dcc2-4cf7-b6a1-75d1b1508033 34 fields · synced May 30, 2026