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ScanAfia X S AM

EUDAMED

Class I (EU MDR)

Ref ScanAfia X S AMModel ScanAfia X hospital beds

by Lojer Oy

Identity

Trade Name
ScanAfia X S AM EUDAMED
Model / Reference
ScanAfia X hospital beds EUDAMED
ScanAfia X S AM EUDAMED

Identifiers

Primary DI / UDI-DI
06430021930033 EUDAMED
Basic UDI-DI
643002193HB0001JH EUDAMED
Direct Marketing DI
06430021930033 EUDAMED
EMDN Code
V08060101 HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

Category: Basic electric hospital bed

Explore the ScanAfia X S AM medical device, designed for hospital beds. Discover its features, including sterile and implantable capabilities, self-testing options, and compliance with industry standards.

Similar devices

Also classified as Basic electric hospital bed.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Lojer Oy
EUDAMED SRN
FI-MF-000001639

Sources (1)

  • EUDAMED 7f0970b0-0cec-419b-9c80-4a8186cb6c4c 61 fields · synced Aug 3, 2026