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Invasive Accessories And Instruments
FDA UDIClass I (US FDA UDI)
by Rhein 83 Srl
Identity
- Trade Name
- INVASIVE ACCESSORIES AND INSTRUMENTS FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- REUSABLE and STERILIZABLE device. Bur with special reverse cutting tip. FDA UDI
- Model / Reference
- SPECIAL BUR FDA UDI
- Description
- REUSABLE and STERILIZABLE device. Bur with special reverse cutting tip. FDA UDI
Identifiers
- Catalog Number
- 780 FDA UDI
- Primary DI / UDI-DI
- D821780 FDA UDI
- FDA Product Code
- DZA FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4130 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Invasive Accessories And Instruments by Rhein 83 Srl — 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
- Rhein 83 Srl
Sources (1)
- FDA UDI 2c01eee8-8007-4204-960e-1aa32ba89098 35 fields · synced May 30, 2026