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Nordema Print IBT

EUDAMED

Class IIa (EU MDR)

Ref 7153

by Nordema GmbH

Identity

Trade Name
Nordema Print IBT EUDAMED
Device Name
Nordema Print IBT EUDAMED
Model / Reference
7153 EUDAMED

Identifiers

Primary DI / UDI-DI
D92671531 EUDAMED
Basic UDI-DI
++D926049410000000049 EUDAMED
EMDN Code
Q010499 ORTHODONTIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa 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

Nordema Print IBT by Nordema GmbH — Class IIa — 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
Nordema GmbH
EUDAMED SRN
DE-MF-000008684

Sources (1)

  • EUDAMED b777a312-9c85-468d-b16b-980e55de9586 61 fields · synced Oct 6, 2026