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Straumann Cares Screw-Retained Bridge Titanium, Dolder Bar Titanium
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- STRAUMANN CARES SCREW-RETAINED BRIDGE TITANIUM, DOLDER BAR TITANIUM FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- Screw-retained Bridge, 7 units, Ti FDA UDI
- Model / Reference
- Bridges (implant borne) FDA UDI
- Description
- Screw-retained Bridge, 7 units, Ti FDA UDI
Identifiers
- Catalog Number
- 010.1081 FDA UDI
- Primary DI / UDI-DI
- 07630031702135 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Conditional FDA UDI
Category: Dental implant suprastructure, permanent, preformed
Straumann Cares Screw-Retained Bridge Titanium, Dolder Bar Titanium by Institut Straumann SA — Class II — FDA UDI — listed in FDA GUDID
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Institut Straumann SA
Sources (1)
- FDA UDI 1fec667a-9293-4c09-bfb2-e804b37b9680 35 fields · synced May 31, 2026