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Archimed

EUDAMED

Class I (EU MDR)

Ref ES00-S SIGMA EMERGENCY STRETCHERModel ES00-S

by Arşi̇med Medi̇kal Kozm.bi̇l.i̇th.i̇hr.paz. Ti̇c.ltd.şti̇.

Identity

Trade Name
ARCHIMED EUDAMED
Device Name
SIGMA EMERGENCY STRETCHER EUDAMED
Model / Reference
ES00-S EUDAMED
ES00-S SIGMA EMERGENCY STRETCHER EUDAMED

Identifiers

Primary DI / UDI-DI
08681957011503 EUDAMED
Basic UDI-DI
86819570186819570115039T EUDAMED
Direct Marketing DI
08681957011503 EUDAMED
EMDN Code
V08050103 EMERGENCY AND TRAUMATOLOGY STRETCHERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Archimed by Arşi̇med Medi̇kal Kozm.bi̇l.i̇th.i̇hr.paz. Ti̇c.ltd.şti̇. — 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

EUDAMED SRN
TR-MF-000036991

Sources (1)

  • EUDAMED e9b2e7d2-a245-4956-bb5a-79cbb9cf618a 61 fields · synced Jun 19, 2026