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Urgent

EUDAMED

Class I (EU MDR)

Ref URGENT

by PROMA REHA, s.r.o.

Identity

Trade Name
URGENT EUDAMED
Device Name
Hospital stretcher EUDAMED
Model / Reference
URGENT EUDAMED

Identifiers

Primary DI / UDI-DI
85942023205998 EUDAMED
Basic UDI-DI
859420232LH01DF EUDAMED
Direct Marketing DI
85942023205998 EUDAMED
EMDN Code
V08050101 GENERIC USE STRETCHERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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

Urgent by PROMA REHA, s.r.o. — 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
PROMA REHA, s.r.o.
EUDAMED SRN
CZ-MF-000013860

Sources (1)

  • EUDAMED 48d07306-a1f2-466e-8a22-5d6b2132b211 61 fields · synced Jul 10, 2026