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CONELOG® Re-Set Removal set
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref C5900.4300
by ALTATEC GmbH
Identity
- Trade Name
- CONELOG® Re-Set Removal set EUDAMEDCONELOG® Re-Set™ FDA UDI
- Generic Name
- Dental implant extractor FDA UDI
- Device Name
- CONELOG® Re-Set EUDAMEDCONELOG® Re-Set™ d 3.8/4.3 mm FDA UDI
- Model / Reference
- C5900.4300 EUDAMEDFDA UDI
- Description
- CONELOG® Re-Set™ d 3.8/4.3 mm FDA UDI
Identifiers
- Catalog Number
- C5900.4300 FDA UDI
- Primary DI / UDI-DI
- 04099797009330 EUDAMEDE219C590043001 FDA UDI
- Basic UDI-DI
- 40997970004002000000000CX EUDAMED
- Secondary DI
- E219C590043001 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 IIa EUDAMEDClass I FDA 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
Yes
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 Removal set by ALTATEC GmbH — Class IIa — 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 | 40997970004002000000000CX | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- ALTATEC GmbH
- EUDAMED SRN
- DE-MF-000006230
Sources (2)
- EUDAMED 1a04cb1e-bca8-4ac2-96aa-bf6f43ecd2f5 61 fields · synced Jul 24, 2026
- FDA UDI 4f5faaa5-757a-42ea-ac2d-58547b7b7002 35 fields · synced May 26, 2026