Identity
- Trade Name
- Occlusinator II Composite Finishing Kit FDA UDI
- Generic Name
- Diamond dental bur, reusable FDA UDI
- Device Name
- Contains : Fine Mini Occlusinator, Standard Acorn Style Bur, and 2.4mm Safe Zone Christmas Tree Burr FDA UDI
- Model / Reference
- 7137551 FDA UDI
- Description
- Contains : Fine Mini Occlusinator, Standard Acorn Style Bur, and 2.4mm Safe Zone Christmas Tree Burr FDA UDI
Identifiers
- Catalog Number
- 7137551 FDA UDI
- Primary DI / UDI-DI
- 00723896011959 FDA UDI
- FDA Product Code
- DZP FDA UDI
- GMDN Term
- Diamond dental bur, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4535 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Occlusinator II Composite Finishing Kit by Practicon, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Practicon, Inc.
Sources (1)
- FDA UDI a2030d50-f80f-43e6-a02d-0d9e99aa4ceb 35 fields · synced Jun 6, 2026