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Epidurální infuzní pumpa Sapphire

EUDAMED

Class IIb (EU MDR)

Ref 15032-000-0015Model Infusion Pump

by Eitan Medical Ltd

Identity

Trade Name
Epidurální infuzní pumpa Sapphire EUDAMED
Device Name
Sapphire Infusion Pump EUDAMED
Model / Reference
Infusion Pump EUDAMED
15032-000-0015 EUDAMED

Identifiers

Primary DI / UDI-DI
07290109155364 EUDAMED
Basic UDI-DI
7290109150001WP EUDAMED
Direct Marketing DI
07290109155364 EUDAMED
EMDN Code
Z12030301 INFUSION PUMPS EUDAMED

Classification

Device Class
Class IIb 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Epidurální infuzní pumpa Sapphire by Eitan Medical Ltd — Class IIb — 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
Eitan Medical Ltd
EUDAMED SRN
IL-MF-000011869
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (1)

  • EUDAMED 0e362331-a558-4b3f-98b5-c09d031b695a 61 fields · synced Jul 24, 2026