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CONELOG® Re-Set Cam ring remover
EUDAMEDFDA UDIClass I (EU MDR)
Ref C5910.4301
by ALTATEC GmbH
Identity
- Trade Name
- CONELOG® Re-Set Cam ring remover EUDAMEDCONELOG® Re-Set™ cam ring remover FDA UDI
- Generic Name
- Dental implant extractor FDA UDI
- Device Name
- CONELOG® RE-Set Cam ring remover EUDAMEDCONELOG® Re-Set™ cam ring remover long for d 3.8/4.3 mm FDA UDI
- Model / Reference
- C5910.4301 EUDAMEDFDA UDI
- Description
- CONELOG® Re-Set™ cam ring remover long for d 3.8/4.3 mm FDA UDI
Identifiers
- Catalog Number
- C5910.4301 FDA UDI
- Primary DI / UDI-DI
- 04099797009385 EUDAMEDE219C591043011 FDA UDI
- Basic UDI-DI
- 40997970006803000000000RN EUDAMED
- Secondary DI
- E219C591043011 EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- Z12110180 INSTRUMENTS FOR DENTAL TREATMENT UNITS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Dental implant extractor 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
Yes
EUDAMEDFDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
CONELOG® Re-Set Cam ring remover 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 | 40997970006803000000000RN | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- ALTATEC GmbH
- EUDAMED SRN
- DE-MF-000006230
Sources (2)
- EUDAMED 9b53ca85-c952-48d7-85c1-2138182fa0f9 61 fields · synced Jun 17, 2026
- FDA UDI 1fb38be2-767b-4768-930a-13d7868b2248 35 fields · synced May 30, 2026