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Kreuzbandage-M

EUDAMED

Class I (EU MDR)

Ref 508330/002/640

by Berkemann Hungary Bt.

Identity

Trade Name
Kreuzbandage-M EUDAMED
Device Name
Talptámasz EUDAMED
Model / Reference
508330/002/640 EUDAMED

Identifiers

Primary DI / UDI-DI
04049261008536 EUDAMED
Basic UDI-DI
4049261TT00YA EUDAMED
Direct Marketing DI
04049261008536 EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) 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

Yes

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: Orthotic insole, prefabricated, non-antimicrobial

Kreuzbandage-M by Berkemann Hungary Bt. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
HU-MF-000007044

Sources (1)

  • EUDAMED be2cdf2e-5c5b-4271-9780-f25cfeff0be3 61 fields · synced Jun 18, 2026