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Model 3 QA Phantom

EUDAMED

Class I (EU MDR)

Ref 13003Model Model 4 Phantom

by Mindways Software, Inc.

Identity

Trade Name
Model 3 QA Phantom EUDAMED
Device Name
Model 4 Phantom EUDAMED
Model / Reference
Model 4 Phantom EUDAMED
13003 EUDAMED

Identifiers

Primary DI / UDI-DI
+B052PHQAM30X EUDAMED
Basic UDI-DI
++B052PHANTOMTU EUDAMED
EMDN Code
Z11900180 BONE DENSITOMETRY SYSTEMS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Model 3 QA Phantom by Mindways Software, Inc. — 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

EUDAMED SRN
US-MF-000012877
Authorised Representative
Johner Medical GmbH DE-AR-000011832

Sources (1)

  • EUDAMED 6274e630-3717-4a13-94e9-d7d946cf2a34 61 fields · synced Jul 20, 2026