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70102a

EUDAMED

Class I (EU MDR)

Ref 70102AModel ScanSleeves Standard Line

by M. G. Kurth GmbH

Identity

Model / Reference
ScanSleeves Standard Line EUDAMED
70102A EUDAMED

Identifiers

Primary DI / UDI-DI
++G08670102A1 EUDAMED
Basic UDI-DI
++G086ScanSleevesLJ EUDAMED
Direct Marketing DI
++G08670102A1 EUDAMED
EMDN Code
T030102 COVER SHEATHS, INSTRUMENTS AND EQUIPMENTS 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

70102a by M. G. Kurth GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
M. G. Kurth GmbH
EUDAMED SRN
DE-MF-000045501

Sources (1)

  • EUDAMED dee60396-8392-4572-9a6b-193cadf34b23 61 fields · synced Jun 18, 2026