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Patient Line

EUDAMED

Class I (EU MDR)

Ref 613415

by Shenzhen Antmed Co., Ltd

Identity

Trade Name
Patient Line EUDAMED
Device Name
Patient Line EUDAMED
Model / Reference
613415 EUDAMED

Identifiers

Primary DI / UDI-DI
06945764438550 EUDAMED
Basic UDI-DI
69457644PL00000015ZW EUDAMED
EMDN Code
A03020102 HIGH PRESSURE EXTENSION LINES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Patient Line by ShenZhen Antmed Co., Ltd — 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
CN-MF-000029659
Authorised Representative
MedNet EC-REP C IIb GmbH DE-AR-000011194

Sources (1)

  • EUDAMED 67a91ed3-d5d7-40c0-a658-0d4323855f6a 61 fields · synced Jun 18, 2026