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MunchiesTM EPS

EUDAMED

Class I (EU MDR)

Ref MunchiesTM EPS

by EOCA MD Pty Ltd

Identity

Device Name
MunchiesTM EPS EUDAMED
Model / Reference
MunchiesTM EPS EUDAMED

Identifiers

Primary DI / UDI-DI
09356117000022 EUDAMED
Basic UDI-DI
09356117000022K7 EUDAMED
Direct Marketing DI
09356117000022 EUDAMED
EMDN Code
Q010499 ORTHODONTIC DEVICES - OTHER 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

MunchiesTM EPS by EOCA MD Pty Ltd — 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
EOCA MD Pty Ltd
EUDAMED SRN
AU-MF-000010294
Authorised Representative
AF Pharma Service Europe SL ES-AR-000018076

Sources (1)

  • EUDAMED 64cb8e82-6cf7-4efd-b4f4-fdfba1e1fe21 61 fields · synced Jul 13, 2026