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Kryckkäpp Flex

EUDAMED

Class I (EU MDR)

Ref 127000Model Crutch

by Swereco AB

Identity

Trade Name
Kryckkäpp Flex EUDAMED
Model / Reference
Crutch EUDAMED
127000 EUDAMED

Identifiers

Primary DI / UDI-DI
07331427270008 EUDAMED
Basic UDI-DI
7331427Y1203MJ EUDAMED
Direct Marketing DI
07331427270008 EUDAMED
EMDN Code
Y12030601 ELBOW CRUTCHES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Kryckkäpp Flex by Swereco AB — 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
Swereco AB
EUDAMED SRN
SE-MF-000033314

Sources (1)

  • EUDAMED 2d50f73c-f3c3-4321-9a1a-1b1a0f5bd2f4 61 fields · synced Aug 3, 2026