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Plasticware

EUDAMED

Class IIa (EU MDR)

Ref 83002

by Kitazato Corporation

Identity

Device Name
Plasticware EUDAMED
Model / Reference
83002 EUDAMED

Identifiers

Primary DI / UDI-DI
14582231462725 EUDAMED
Basic UDI-DI
458223146PLWL5 EUDAMED
EMDN Code
U080206 CULTURE PLATES FOR ASSISTED REPRODUCTION EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

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

Plasticware by Kitazato Corporation — Class IIa — 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
JP-MF-000018374
Authorised Representative
BIOMEDICAL SUPPLY, S.L. ES-AR-000014358

Sources (1)

  • EUDAMED c6b1cc8b-e8e2-44e4-97c2-febd703fd3f5 61 fields · synced Jun 18, 2026