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VueBox GI-Perfusion Version 8

EUDAMED

Class IIa (EU MDR)

Ref 680029

by Bracco Suisse Sa

Identity

Trade Name
VueBox GI-Perfusion Version 8 EUDAMED
Device Name
VueBox EUDAMED
Model / Reference
680029 EUDAMED

Identifiers

Primary DI / UDI-DI
07649996041067 EUDAMED
Basic UDI-DI
7649996041VueBoxRF EUDAMED
EMDN Code
V92 MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software 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

VueBox GI-Perfusion Version 8 by Bracco Suisse Sa — 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
Bracco Suisse Sa
EUDAMED SRN
CH-MF-000022733
Authorised Representative
ACIST Europe BV NL-AR-000002151

Sources (1)

  • EUDAMED fc3ed022-4f4a-4678-a7bc-edc53ae99b75 61 fields · synced Jul 8, 2026