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IMPROSAFE® Blood Collection Set

EUDAMED

Class IIa (EU MDR)

Ref 596122300Model 21G × 3/4” × 12”; 22G × 3/4ʺ × 12ʺ; 23G × 3/4” × 12”; 24G × 3/4ʺ × 12ʺ; 25G × 3/4” × 12”; 21G × 3/4” × 7”; 22G × 3/4ʺ × 7ʺ; 23G × 3/4” × 7”; 24G × 3/4ʺ × 7ʺ; 25G × 3/4” × 7”

by Guangzhou Improve Medical Instruments Co., Ltd

Identity

Trade Name
IMPROSAFE® Blood Collection Set EUDAMED
Device Name
IMPROSAFE® Blood Collection Set EUDAMED
Model / Reference
21G × 3/4” × 12”; 22G × 3/4ʺ × 12ʺ; 23G × 3/4” × 12”; 24G × 3/4ʺ × 12ʺ; 25G × 3/4” × 12”; 21G × 3/4” × 7”; 22G × 3/4ʺ × 7ʺ; 23G × 3/4” × 7”; 24G × 3/4ʺ × 7ʺ; 25G × 3/4” × 7” EUDAMED
596122300 EUDAMED

Identifiers

Primary DI / UDI-DI
06974481831634 EUDAMED
Basic UDI-DI
697448183001004UW EUDAMED
EMDN Code
A010199 NEEDLES FOR INFUSION AND COLLECTION - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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® 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 866f2ee0-b9d6-4fa9-9d9f-e257bb2cc9a8 61 fields · synced May 29, 2026