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CAMLOG® Temporary abutment
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref K2239.6000
by ALTATEC GmbH
Identity
- Trade Name
- CAMLOG® Temporary abutment EUDAMEDCAMLOG® Temporary abutment (titanium) FDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
- Device Name
- CAMLOG® Temporary abutment, crown EUDAMEDK2239.6000 CAMLOG® Temporary abutment (titanium) d= 6.0 mm FDA UDI
- Model / Reference
- K2239.6000 EUDAMEDFDA UDI
- Description
- K2239.6000 CAMLOG® Temporary abutment (titanium) d= 6.0 mm FDA UDI
Identifiers
- Catalog Number
- K2239.6000 FDA UDI
- Primary DI / UDI-DI
- 04099797006889 EUDAMEDE219K223960001 FDA UDI
- Basic UDI-DI
- 40997970001109000000000GL EUDAMED
- Secondary DI
- E219K223960001 EUDAMED
- FDA Product Code
- NHA FDA UDI
- EMDN Code
- P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
- GMDN Term
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Sutures
Yes
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
CAMLOG® Temporary abutment by ALTATEC GmbH — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 40997970001109000000000GL | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- ALTATEC GmbH
- EUDAMED SRN
- DE-MF-000006230
Sources (2)
- EUDAMED ff4a2636-15ac-48fd-9feb-7e9e3b165b5a 61 fields · synced Jul 9, 2026
- FDA UDI ba6d7729-3758-49cb-a233-c42bee8fe851 35 fields · synced May 30, 2026