Ot Equator-Ot Bridge
FDA UDIEUDAMEDClass I (US FDA UDI)
by Rhein 83 Srl
Identity
- Trade Name
- TRANSFER TITANIO OT BRIDGE h6 EUDAMEDOT EQUATOR-OT BRIDGE FDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
- Device Name
- TRANSFER + VITE per STRAUMANN EUDAMED
- Model / Reference
- 144TTE EUDAMEDOT EQUATOR SHORT IMPRESS. COPING W/SCREW FDA UDI
Identifiers
- Catalog Number
- 144TTE FDA UDI
- Primary DI / UDI-DI
- 08059224107998 EUDAMEDFDA UDI
- Basic UDI-DI
- 805804571TRTPE EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED
- GMDN Term
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
Yes
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Dental implant suprastructure, temporary, preformed, single-use
Ot Equator-Ot Bridge by Rhein 83 Srl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant suprastructure, temporary, preformed, single-use.
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- Impression Coping — ARUM DENTISTRY Co., Ltd. · Class I
- Neoss Implant System — Neoss, Ltd. · Class II
- Scanbody Screw — ARUM DENTISTRY Co., Ltd. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Rhein 83 Srl
Sources (2)
- FDA UDI 7ab047f0-cb04-451e-bb97-cf376b0a553e 33 fields · synced Jul 14, 2026
- EUDAMED f129e5cf-29f1-47e4-a86b-034151f2cb39 61 fields · synced Jul 14, 2026