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imagiQ2

EUDAMED

Class I (EU MDR)

Ref 530-1700

by Stille AB

Identity

Trade Name
imagiQ2 EUDAMED
Device Name
imagiQ2 EUDAMED
Model / Reference
530-1700 EUDAMED

Identifiers

Primary DI / UDI-DI
07332339222086 EUDAMED
Basic UDI-DI
733233953079 EUDAMED
Direct Marketing DI
07332339222086 EUDAMED
EMDN Code
V08060199 ELECTRIC MEDICAL BEDS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

imagiQ2 by Stille AB — 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
Stille AB
EUDAMED SRN
SE-MF-000001228

Sources (1)

  • EUDAMED f6711eb7-ebb9-4929-b907-3f74baea661c 61 fields · synced May 25, 2026