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Adult Reusable Inductive System Kit / Nox Compatible
EUDAMEDClass I (EU MDR)
Ref 9010NX-KitModel 9XXX, 9XXX-LXX, 501-0261-X series
by S.L.P. Ltd.
Identity
- Trade Name
- Adult Reusable Inductive System Kit / Nox Compatible EUDAMED
- Device Name
- Inductive Sensors EUDAMED
- Model / Reference
- 9XXX, 9XXX-LXX, 501-0261-X series EUDAMED9010NX-Kit EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07290016715941 EUDAMED
- Basic UDI-DI
- 7290001671EF001L7 EUDAMED
- EMDN Code
- Z1399 NON-SPECIFIC CONSUMABLES FOR DIAGNOSTIC INSTRUMENTS - 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
Adult Reusable Inductive System Kit / Nox Compatible by S.L.P. Ltd. — Class I — 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 | 7290001671EF001L7 | Class I | Active |
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Manufacturer
- Manufacturer
- S.L.P. Ltd.
- EUDAMED SRN
- IL-MF-000016600
- Authorised Representative
- Arazy Group GmbH DE-AR-000007685
Sources (1)
- EUDAMED 52afa7cc-5ba9-4962-8339-9508c6211c9f 61 fields · synced Jul 12, 2026