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Sapphire-epiduraali-i nfuusi opump

EUDAMED

Class IIb (EU MDR)

Ref 15032-000-0017Model Infusion Pump

by Eitan Medical Ltd

Identity

Trade Name
Sapphire-epiduraali-i nfuusi opump EUDAMED
Device Name
Sapphire Infusion Pump EUDAMED
Model / Reference
Infusion Pump EUDAMED
15032-000-0017 EUDAMED

Identifiers

Primary DI / UDI-DI
07290109155562 EUDAMED
Basic UDI-DI
7290109150001WP EUDAMED
Direct Marketing DI
07290109155562 EUDAMED
EMDN Code
Z12030301 INFUSION PUMPS EUDAMED

Classification

Device Class
Class IIb 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sapphire-epiduraali-i nfuusi opump 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 e34d0088-01ce-4973-98c7-5e4e028bb8b5 61 fields · synced Jun 17, 2026