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easyEndo™ UniPlus Single Use Reload

EUDAMED

Class IIb (EU MDR)

Ref P60XT

by Ezisurg Medical Co., Ltd.

Identity

Trade Name
easyEndo™ UniPlus Single Use Reload EUDAMED
Device Name
Single Use Reloads EUDAMED
Model / Reference
P60XT EUDAMED

Identifiers

Primary DI / UDI-DI
06925776123415 EUDAMED
Basic UDI-DI
69257761002503Y7 EUDAMED
EMDN Code
H0202010301,H02030106 EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

Yes

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

easyEndo™ UniPlus Single Use Reload by Ezisurg Medical Co., 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

EUDAMED SRN
CN-MF-000006742
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 4d737611-b9b7-45f1-944a-4bdb03fc1513 61 fields · synced Jul 30, 2026