← Back to catalogue
CAMLOG® Gingiva height Indicator
EUDAMEDFDA UDIClass I (EU MDR)
Ref J3550.3800
by ALTATEC GmbH
Identity
- Trade Name
- CAMLOG® Gingiva height Indicator EUDAMEDGingiva height indicator FDA UDI
- Generic Name
- Dental implantation depth/angle gauge, reusable FDA UDI
- Device Name
- Dental implantation depth/angle gauge, reusable EUDAMEDGingiva height indicator, for Ø 3.8 mm FDA UDI
- Model / Reference
- J3550.3800 EUDAMEDFDA UDI
- Description
- Gingiva height indicator, for Ø 3.8 mm FDA UDI
Identifiers
- Catalog Number
- J3550.3800 FDA UDI
- Primary DI / UDI-DI
- 04099797997392 EUDAMEDE219J355038001 FDA UDI
- Basic UDI-DI
- 40997970008007000000000NL EUDAMED
- Secondary DI
- E219J355038001 EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- Z12110180 INSTRUMENTS FOR DENTAL TREATMENT UNITS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Dental implantation depth/angle gauge, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
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
Yes
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® Gingiva height Indicator by ALTATEC GmbH — Class I — 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 | 40997970008007000000000NL | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | 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 d71540f2-febb-4822-a18f-47af2743bcc5 61 fields · synced Jul 12, 2026
- FDA UDI 45ed89df-bd9d-4028-8e69-078bc1a8a6bc 35 fields · synced May 30, 2026