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IMPROVACUTER® Blood Collection Set

EUDAMED

Class IIa (EU MDR)

Ref 594125300Model 20G×3/4ʺ×7ʺ;21G×3/4″×7″;22G×3/4″×7″;23G×3/4″×7″;24G×3/4ʺ×7ʺ;25G×3/4″×7″;20G×3/4ʺ×12ʺ;21G×3/4″×12″;22G×3/4ʺ×12″;23G×3/4″×12″;24G×3/4ʺ×12ʺ;25G×3/4″×12″

by Guangzhou Improve Medical Instruments Co., Ltd

Identity

Trade Name
IMPROVACUTER® Blood Collection Set EUDAMED
Device Name
Blood Collection Needle EUDAMED
Model / Reference
20G×3/4ʺ×7ʺ;21G×3/4″×7″;22G×3/4″×7″;23G×3/4″×7″;24G×3/4ʺ×7ʺ;25G×3/4″×7″;20G×3/4ʺ×12ʺ;21G×3/4″×12″;22G×3/4ʺ×12″;23G×3/4″×12″;24G×3/4ʺ×12ʺ;25G×3/4″×12″ EUDAMED
594125300 EUDAMED

Identifiers

Primary DI / UDI-DI
06974481838886 EUDAMED
Basic UDI-DI
697448183001003UU EUDAMED
EMDN Code
A010199 NEEDLES FOR INFUSION AND COLLECTION - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Cyprus 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

IMPROVACUTER® Blood Collection Set 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 36f09d41-f705-4ae2-9b06-cebcd788d230 61 fields · synced May 29, 2026