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Anti Bed-Sore Foam Mattress Kuba

EUDAMED

Class I (EU MDR)

Ref KUBA

by UAB Kasko Group

Identity

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

Identifiers

Primary DI / UDI-DI
04779031631373 EUDAMED
Basic UDI-DI
477903163KUBAJX EUDAMED
Direct Marketing DI
04779031631373 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

Anti Bed-Sore Foam Mattress Kuba 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

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Manufacturer

Manufacturer
UAB Kasko Group
EUDAMED SRN
LT-MF-000007721

Sources (1)

  • EUDAMED af06dd32-921d-452f-84ea-0406aeabe3aa 61 fields · synced Jun 18, 2026