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IMPROSAFE® Multi Sample Needle

EUDAMED

Class IIa (EU MDR)

Ref 598120250Model 20G × 1ʺ; 20G × 1 1/2ʺ; 21G × 1″; 21G × 1 1/2″; 22G × 1″; 22G × 1 1/2″; 23G × 1ʺ; 23G × 1 1/2ʺ

by Guangzhou Improve Medical Instruments Co., Ltd

Identity

Trade Name
IMPROSAFE® Multi Sample Needle EUDAMED
Device Name
IMPROSAFE® Multi Sample Needle EUDAMED
Model / Reference
20G × 1ʺ; 20G × 1 1/2ʺ; 21G × 1″; 21G × 1 1/2″; 22G × 1″; 22G × 1 1/2″; 23G × 1ʺ; 23G × 1 1/2ʺ EUDAMED
598120250 EUDAMED

Identifiers

Primary DI / UDI-DI
06974481831702 EUDAMED
Basic UDI-DI
697448183001002US EUDAMED
EMDN Code
A010199 NEEDLES FOR INFUSION AND COLLECTION - OTHER EUDAMED

Classification

Device Class
Class IIa 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

IMPROSAFE® Multi Sample Needle by Guangzhou Improve Medical Instruments 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-000006536
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED b54e5f77-ce55-4b3a-acbb-66d04abf0f1e 61 fields · synced May 29, 2026