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Lt

EUDAMED

Class I (EU MDR)

Ref 32-040Model Leak Tester Main

by SMART Medical Systems Ltd.

Identity

Trade Name
LT EUDAMED
Device Name
Leak Tester EUDAMED
Model / Reference
Leak Tester Main EUDAMED
32-040 EUDAMED

Identifiers

Primary DI / UDI-DI
07290018671573 EUDAMED
Basic UDI-DI
7290018671LTGS EUDAMED
Direct Marketing DI
07290018671573 EUDAMED
EMDN Code
G0380 DIGESTIVE ENDOSCOPY DEVICES - ACCESSORIES 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: Gastro-urological guidewire, single-use

Lt by Smart Medical Systems Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gastro-urological guidewire, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IL-MF-000011336
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 745b2431-bc8f-4771-84e4-e58493e15d26 61 fields · synced Jun 14, 2026