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Sandegårds madrass

EUDAMED

Class I (EU MDR)

Ref QT 2025 – 002

by Hjärtshopen AB

Identity

Trade Name
Sandegårds madrass EUDAMED
Device Name
Sandegårds Madrass EUDAMED
Model / Reference
QT 2025 – 002 EUDAMED

Identifiers

Primary DI / UDI-DI
07350178580020 EUDAMED
Basic UDI-DI
7350178582025002EL EUDAMED
Direct Marketing DI
07350178580020 EUDAMED
EMDN Code
M03050299 BANDAGES AND SPLINTS - 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

Sandegårds madrass by Hjärtshopen 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
Hjärtshopen AB
EUDAMED SRN
SE-MF-000048486

Sources (1)

  • EUDAMED fcf2ecb5-37ca-4926-802d-1de4603ac562 61 fields · synced Jun 18, 2026