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Sb®910

EUDAMED

Class I (EU MDR)

Ref 3000910-GA231BT

by Invacare Rea AB

Identity

Trade Name
SB®910 EUDAMED
Device Name
SB®910 EUDAMED
Model / Reference
3000910-GA231BT EUDAMED

Identifiers

Primary DI / UDI-DI
07323410137436 EUDAMED
Basic UDI-DI
7331226SB910ND EUDAMED
EMDN Code
V08060101 HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS 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

Sb®910 by Invacare Rea 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
Invacare Rea AB
EUDAMED SRN
SE-MF-000003772

Sources (1)

  • EUDAMED 24cad2c2-c44e-4384-b633-ad1b6d5649a0 61 fields · synced Jun 20, 2026