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Emergo 6250

EUDAMED

Class I (EU MDR)

Ref Emergo 6250Model Emergo Emergency and patient trolleys

by Lojer Oy

Identity

Trade Name
Emergo 6250 EUDAMED
Model / Reference
Emergo Emergency and patient trolleys EUDAMED
Emergo 6250 EUDAMED

Identifiers

Primary DI / UDI-DI
06430021930224 EUDAMED
Basic UDI-DI
643002193TS0001V8 EUDAMED
Direct Marketing DI
06430021930224 EUDAMED
EMDN Code
V08050103 EMERGENCY AND TRAUMATOLOGY STRETCHERS 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

Emergo 6250 by Lojer Oy — 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
Lojer Oy
EUDAMED SRN
FI-MF-000001639

Sources (1)

  • EUDAMED 8812cc9a-2459-4b5c-bc08-82ac2ef897b6 61 fields · synced Jun 19, 2026