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Edge Sequel Sapphire
EUDAMEDClass IIa (EU MDR)
Ref ES500421HTSModel S1.7B0.00.0FI.FK
Identity
- Trade Name
- EDGE SEQUEL SAPPHIRE EUDAMED
- Device Name
- R-Motion EUDAMED
- Model / Reference
- S1.7B0.00.0FI.FK EUDAMEDES500421HTS EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640452461900 EUDAMED
- Basic UDI-DI
- 7640142410401019R EUDAMED
- EMDN Code
- Q010507 ENDODONTIC INSTRUMENTS (CANAL ENLARGERS, FILES, RASPS, ETC.), SINGLE-USE EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
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
Edge Sequel Sapphire by FKG Dentaire Sàrl — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
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 | 7640142410401019R | Class IIa | Active |
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Manufacturer
- Manufacturer
- FKG Dentaire Sàrl
- EUDAMED SRN
- CH-MF-000017925
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED ceeb9c2e-21f1-41ea-9455-11d6ed3c278a 61 fields · synced Jun 19, 2026