← Back to catalogue

Reusable Inductive System, Adult - Key Connector

EUDAMED

Class I (EU MDR)

Ref 9010E-KitModel 9XXX, 9XXX-LXX, 501-0261-X series

by S.L.P. Ltd.

Identity

Trade Name
Reusable Inductive System, Adult - Key Connector EUDAMED
Device Name
Inductive Sensors EUDAMED
Model / Reference
9XXX, 9XXX-LXX, 501-0261-X series EUDAMED
9010E-Kit EUDAMED

Identifiers

Primary DI / UDI-DI
07290016715132 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

Reusable Inductive System, Adult - Key Connector 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
S.L.P. Ltd.
EUDAMED SRN
IL-MF-000016600
Authorised Representative
Arazy Group GmbH DE-AR-000007685

Sources (1)

  • EUDAMED 8b3d0f7e-e8b6-4a2c-bc23-9035fb5bded5 61 fields · synced Jun 20, 2026