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Injection Tubing System

EUDAMED

Class IIa (EU MDR)

Ref 804102

by Shenzhen Antmed Co., Ltd

Identity

Trade Name
Injection Tubing System EUDAMED
Device Name
Injection Tubing System EUDAMED
Model / Reference
804102 EUDAMED

Identifiers

Primary DI / UDI-DI
06945764431407 EUDAMED
Basic UDI-DI
69457644ITS0000005MH EUDAMED
EMDN Code
A03020102 HIGH PRESSURE EXTENSION LINES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

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

Sources (1)

  • EUDAMED c0c796b4-20e6-4e88-8ff6-8fc9b2322631 61 fields · synced Jun 18, 2026