Identity
- Trade Name
- FINISHING KIT FDA UDI
- Generic Name
- Dental abrasive disk, reusable FDA UDI
- Model / Reference
- N-71000P FDA UDI
Identifiers
- Catalog Number
- N-71000P FDA UDI
- Primary DI / UDI-DI
- D757N71000P1 FDA UDI
- FDA Product Code
- DZN FDA UDI
- GMDN Term
- Dental abrasive disk, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Finishing Kit by Bisco 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
- Bisco Inc.
Sources (1)
- FDA UDI b3d1132a-843d-47ba-8640-2e9f571425e3 36 fields · synced Jun 8, 2026