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Archimed

EUDAMED

Class I (EU MDR)

Ref ES40-A NOVA ACİL EMERGENCY STRETCHERModel ES20-S

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

Identity

Trade Name
ARCHIMED EUDAMED
Device Name
S-STONE BARIATRIC EMERGENCY STRETCHER EUDAMED
Model / Reference
ES20-S EUDAMED
ES40-A NOVA ACİL EMERGENCY STRETCHER EUDAMED

Identifiers

Primary DI / UDI-DI
08681957013651 EUDAMED
Basic UDI-DI
8681957013460CA EUDAMED
Direct Marketing DI
08681957013651 EUDAMED
EMDN Code
V08050103 EMERGENCY AND TRAUMATOLOGY STRETCHERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye 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 ca43e49d-1324-447d-b24d-d155c686f907 61 fields · synced Jun 18, 2026