← Back to catalogue

Visko

EUDAMED

Class I (EU MDR)

Ref VISKO

by UAB Kasko Group

Identity

Trade Name
VISKO EUDAMED
Device Name
ANTI BED-SORE FOAM MATTRESS VISKO EUDAMED
Model / Reference
VISKO EUDAMED

Identifiers

Primary DI / UDI-DI
04779031632929 EUDAMED
Basic UDI-DI
477903163VISKONK EUDAMED
Direct Marketing DI
04779031632929 EUDAMED
EMDN Code
V080702 NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Lithuania 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

Visko by UAB Kasko Group — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
UAB Kasko Group
EUDAMED SRN
LT-MF-000007721

Sources (1)

  • EUDAMED 1a4b9a34-09a1-42ef-823b-0de79ebafe2c 61 fields · synced Jun 19, 2026