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X-ray film viewer Box

EUDAMED

Class I (EU MDR)

Ref D1 Model D1,D2,D3,D4,LED-T1,LED-T2,LED-T3,LED-T4,D1B,D2B,D3B,D4B

by Hefei Mt Medical Co., Ltd.

Identity

Device Name
X-ray film viewer Box EUDAMED
Model / Reference
D1,D2,D3,D4,LED-T1,LED-T2,LED-T3,LED-T4,D1B,D2B,D3B,D4B EUDAMED
D1 EUDAMED

Identifiers

Primary DI / UDI-DI
06978858979509 EUDAMED
Basic UDI-DI
697885897xvb0104S EUDAMED
EMDN Code
Z11079099 VARIOUS X–RAY FILM IMAGING SUPPORT INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

X-ray film viewer Box by Hefei Mt Medical Co., 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

EUDAMED SRN
CN-MF-000008983
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED b4be041b-ba61-4f57-86e4-0ff80bb4185c 61 fields · synced Jul 30, 2026