← Back to catalogue

70200

EUDAMED

Class I (EU MDR)

Ref 70200Model ScanSleeves Standard Line

by M. G. Kurth GmbH

Identity

Model / Reference
ScanSleeves Standard Line EUDAMED
70200 EUDAMED

Identifiers

Primary DI / UDI-DI
++G086702001 EUDAMED
Basic UDI-DI
++G086ScanSleevesLJ EUDAMED
Direct Marketing DI
++G086702001 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

70200 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

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

Manufacturer

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

Sources (1)

  • EUDAMED f8a14555-6a34-407f-b9c0-6676e59d2147 61 fields · synced Jul 13, 2026