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I-Ha4130

EUDAMED

Class I (EU MDR)

Ref 250988

by provita medical gmbh & co. kg

Identity

Trade Name
I-HA4130 EUDAMED
Device Name
IV-stand mobile + accessories EUDAMED
Model / Reference
250988 EUDAMED

Identifiers

Primary DI / UDI-DI
04260123935283 EUDAMED
Basic UDI-DI
42601239302J6 EUDAMED
Direct Marketing DI
04260123935283 EUDAMED
EMDN Code
Z12030380 INFUSION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

I-Ha4130 by provita medical gmbh & co. kg — 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
DE-MF-000005332

Sources (1)

  • EUDAMED 2ea5b348-9fc4-4300-a907-f27c26a6db8a 61 fields · synced Oct 7, 2026