Identity
- Trade Name
- DENTAL EQUIPMENTS FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- SINGLE USE castable device, titanium threaded sleeve and titanium sphere with nitride coating to be transformed via casting technique in a metal attachment for removable prosthesis. FDA UDI
- Model / Reference
- YELLOW CAPS STANDARD size100u. FDA UDI
- Description
- SINGLE USE castable device, titanium threaded sleeve and titanium sphere with nitride coating to be transformed via casting technique in a metal attachment for removable prosthesis. FDA UDI
Identifiers
- Catalog Number
- CN003-100 FDA UDI
- Primary DI / UDI-DI
- D821CN003100 FDA UDI
- FDA Product Code
- EGG FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3165 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
Dental Equipments 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 7cb582a0-cd2b-47f3-9349-230e4696c5e3 35 fields · synced May 31, 2026