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Epidural anesthesia kit

EUDAMED

Class III (EU MDR)

Ref EKT1790181Model AS-E

by Zhejiang Runqiang Medical Instruments Co., Ltd

Identity

Trade Name
Epidural anesthesia kit EUDAMED
Device Name
Disposable Anaesthesia Needle and Anaesthesia Kit EUDAMED
Model / Reference
AS-E EUDAMED
EKT1790181 EUDAMED

Identifiers

Primary DI / UDI-DI
06973740676917 EUDAMED
Basic UDI-DI
697374067001LF EUDAMED
Direct Marketing DI
06973740676917 EUDAMED
EMDN Code
A01030102 EPIDURAL ANAESTHESIA NEEDLES AND KITS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

Yes

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Epidural anesthesia kit by Zhejiang Runqiang Medical Instruments Co., Ltd — Class III — 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-000005693
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 09ae6645-4fa7-4aa5-af42-22b30370e888 61 fields · synced Oct 6, 2026