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Daiwha Corp., Ltd.

EUDAMED

Class IIb (EU MDR)

Ref DW-56Model DS-5000

by Daiwha Corp., Ltd.

Identity

Trade Name
Daiwha Corp., Ltd. EUDAMED
Device Name
MEDIFUSION EUDAMED
Model / Reference
DS-5000 EUDAMED
DW-56 EUDAMED

Identifiers

Primary DI / UDI-DI
08800009400441 EUDAMED
Basic UDI-DI
B-08800009400441 EUDAMED
EMDN Code
Z12030302 SYRINGE PUMPS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Daiwha Corp., Ltd. by Daiwha Corp., Ltd. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Daiwha Corp., Ltd.
EUDAMED SRN
KR-MF-000024402
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED 860642c5-ab90-40de-8490-116122faa900 61 fields · synced Jun 18, 2026