Identity
- Trade Name
- DENTAL EQUIPMENTS FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- 022OBB - SINGLE USE castable device: Bar with a retentive profile. 025CPB - SINGLE USE castable device. Prefabricated housing for bar. 023CPA - SINGLE USE castable device. Prefabricated positioner for castable box. 024CPB - SINGLE USE castable device. Prefabricated positioner for castable box. 027CRG - DISPOSABLE device in plastic material to be embodied in a removable prosthesis. Cap with average retention. 026CRR - DISPOSABLE device in plastic material to be embodied in a removable prosthesis. Clip with soft retention 027CRS - DISPOSABLE device in plastic material to be embodied in a removable prosthesis. Clip with extra soft retention 022RGO - SINGLE USE castable device. Prefabricated reinforcement bar. 155CC - SINGLE USE castable device Connector for castable housings FDA UDI
- Model / Reference
- OT BAR MULTIUSE x USA FDA UDI
- Description
- 022OBB - SINGLE USE castable device: Bar with a retentive profile. 025CPB - SINGLE USE castable device. Prefabricated housing for bar. 023CPA - SINGLE USE castable device. Prefabricated positioner for castable box. 024CPB - SINGLE USE castable device. Prefabricated positioner for castable box. 027CRG - DISPOSABLE device in plastic material to be embodied in a removable prosthesis. Cap with average retention. 026CRR - DISPOSABLE device in plastic material to be embodied in a removable prosthesis. Clip with soft retention 027CRS - DISPOSABLE device in plastic material to be embodied in a removable prosthesis. Clip with extra soft retention 022RGO - SINGLE USE castable device. Prefabricated reinforcement bar. 155CC - SINGLE USE castable device Connector for castable housings FDA UDI
Identifiers
- Catalog Number
- 021OBMUS FDA UDI
- Primary DI / UDI-DI
- 08059224015682 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
- 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Liquid Chemical FDA UDI
Category: Dental implant suprastructure, permanent, preformed
Dental Equipments by Rhein 83 Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant suprastructure, permanent, preformed.
- SPARE CAST. SLEEVE FOR — SWEDEN & MARTINA INC · Class II
- HS/HG Prosthetic System — OSSTEM IMPLANT Co., Ltd. · Class II
- DESS dental smart solutions — TERRATS MEDICAL SL. · Class II
- Diamodent — Diamodent · Class II
- Cemented Abutment — POINTIMPLANT Co., Ltd. · Class II
- GS System — OSSTEM IMPLANT Co., Ltd. · Class II
- Temporary Abutment — Cybermed Inc. · Class II
- EZ Post — Megagen Implant Co. Ltd · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Rhein 83 Srl
Sources (1)
- FDA UDI f932c371-403b-4f66-9687-b8106a2db5b7 34 fields · synced May 30, 2026