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CAMLOG® Healing cap
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref K2004.5040
by ALTATEC GmbH
Identity
- Trade Name
- CAMLOG® Healing cap EUDAMEDCAMLOG® Healing Cap PS FDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
- Device Name
- CAMLOG® Healing cap EUDAMEDK2004.5040 CAMLOG® Healing Cap PS, wide body Ø 5.0 GH 4.0 FDA UDI
- Model / Reference
- K2004.5040 EUDAMEDFDA UDI
- Description
- K2004.5040 CAMLOG® Healing Cap PS, wide body Ø 5.0 GH 4.0 FDA UDI
Identifiers
- Catalog Number
- K2004.5040 FDA UDI
- Primary DI / UDI-DI
- 04099797005943 EUDAMEDE219K200450401 FDA UDI
- Basic UDI-DI
- 40997970002101000000000AM EUDAMED
- Secondary DI
- E219K200450401 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
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
CAMLOG® Healing cap 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 | 40997970002101000000000AM | 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 83ec23ce-5257-4b9d-b1f0-df5aa59423c5 61 fields · synced May 31, 2026
- FDA UDI 9f92f069-e908-437b-b04e-c30e6054788d 35 fields · synced May 30, 2026