Identity
- Trade Name
- UP 5020 / KFO3 EUDAMED
- Device Name
- Versorgungselement EUDAMED
- Model / Reference
- 832610 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04260746660623 EUDAMED
- Basic UDI-DI
- 426074666UD7330573 EUDAMED
- Direct Marketing DI
- 04260746660623 EUDAMED
- EMDN Code
- Z12110101 DENTAL TREATMENT UNITS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
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
Category: Dental delivery system
Up 5020 / Kfo3 by Ultradent Dental-Medizinische-Geräte GmbH & Co KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 426074666UD7330573 | Class I | Active |
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Manufacturer
- Manufacturer
- Ultradent Dental-Medizinische-Geräte GmbH & Co KG
- EUDAMED SRN
- DE-MF-000020027
Sources (1)
- EUDAMED f4f72bcc-c3eb-47f5-83c2-ec507d31aa85 61 fields · synced Jul 15, 2026