← Back to catalogue
CAMLOG® Abutment screw
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref J4005.2001
by ALTATEC GmbH
Identity
- Trade Name
- CAMLOG® Abutment screw EUDAMEDCAMLOG® Abutment screw FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- CAMLOG® Abutment screw, hex EUDAMEDJ4005.2001 CAMLOG® Abutment screw, hex d 5.0/6.0 mm, thread M 2.0 FDA UDI
- Model / Reference
- J4005.2001 EUDAMEDFDA UDI
- Description
- J4005.2001 CAMLOG® Abutment screw, hex d 5.0/6.0 mm, thread M 2.0 FDA UDI
Identifiers
- Catalog Number
- J4005.2001 FDA UDI
- Primary DI / UDI-DI
- 04099797004229 EUDAMEDE219J400520011 FDA UDI
- Basic UDI-DI
- 40997970001111000000000AB EUDAMED
- Secondary DI
- E219J400520011 EUDAMED
- FDA Product Code
- NHA FDA UDI
- EMDN Code
- P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
- GMDN Term
- Dental implant suprastructure, permanent, preformed 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® Abutment screw 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
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 40997970001111000000000AB | Class IIb | Active |
| EUDAMED | European Union | CE/MDR | 40997970001111000000000AB | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- ALTATEC GmbH
- EUDAMED SRN
- DE-MF-000006230
Sources (2)
- EUDAMED fcf0a0ab-3ee1-4c2e-8f0d-b6435f6de973 61 fields · synced May 31, 2026
- FDA UDI a4c11a40-dd66-4d54-9776-8f3fc2e1dfc9 35 fields · synced May 29, 2026