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CAMLOG® Re-Set Removal set
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref J5900.3300
by ALTATEC GmbH
Identity
- Trade Name
- CAMLOG® Re-Set Removal set EUDAMEDCAMLOG® Re-Set FDA UDI
- Generic Name
- Dental implant extractor FDA UDI
- Device Name
- CAMLOG® Re-Set EUDAMEDCAMLOG® Re-Set d 3.3 mm FDA UDI
- Model / Reference
- J5900.3300 EUDAMEDFDA UDI
- Description
- CAMLOG® Re-Set d 3.3 mm FDA UDI
Identifiers
- Catalog Number
- J5900.3300 FDA UDI
- Primary DI / UDI-DI
- 04099797013405 EUDAMEDE219J590033001 FDA UDI
- Basic UDI-DI
- 40997970004028000000000LB EUDAMED
- Secondary DI
- E219J590033001 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
CAMLOG® 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 | 40997970004028000000000LB | 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 768dfaa3-c6ca-4970-99fd-45b6e63a8102 61 fields · synced Jul 30, 2026
- FDA UDI 2252e422-86e8-468f-8a2f-9ec4282afec4 35 fields · synced May 30, 2026