Identity
- Trade Name
- Crown cutter FDA UDI
- Generic Name
- Diamond dental bur, reusable FDA UDI
- Device Name
- ZIRCUT crown cutter HP, pu: 1 pc FDA UDI
- Model / Reference
- 940702 FDA UDI
- Description
- ZIRCUT crown cutter HP, pu: 1 pc FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04057176151155 FDA UDI
- FDA Product Code
- EJL FDA UDI
- GMDN Term
- Diamond dental bur, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3240 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Category: Diamond dental bur, reusable
Crown cutter by DFS - DIAMON GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Diamond dental bur, reusable.
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- HORICO — Hopf, Ringleb & Co. GmbH & Cie. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- DFS - DIAMON GmbH
Sources (1)
- FDA UDI d690ce52-d292-4ab6-a2bd-0a41c19983ee 33 fields · synced Jun 8, 2026