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SKYDOQ® Spring Arm24
EUDAMEDClass I (EU MDR)
Ref 7500-07-00-0076-910
by AMTRION GmbH
Identity
- Device Name
- SKYDOQ® Spring Arm24 EUDAMED
- Model / Reference
- 7500-07-00-0076-910 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04260217225214 EUDAMED
- Basic UDI-DI
- 426021722-FA24-0000-FN EUDAMED
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER 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: Device sterilization/disinfection container, reusable
SKYDOQ® Spring Arm24 by AMTRION GmbH — 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 | 426021722-FA24-0000-FN | Class I | Active |
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Manufacturer
- Manufacturer
- AMTRION GmbH
- EUDAMED SRN
- DE-MF-000029547
Sources (1)
- EUDAMED 100a2fcd-1691-4a54-96be-c25ab95f70d5 61 fields · synced Sep 30, 2026