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IMPROSAFE® ImPress Blood Collection Set

EUDAMED

Class IIa (EU MDR)

Ref 5991253002Model 25G×3/4×7″ TW;25G×3/4×12″ TW;23G×3/4×7″ TW;23G×3/4×12″ TW;21G×3/4×7″ TW;21G×3/4×12″ TW;25G×3/4×7″ UTW;25G×3/4×12″ UTW;23G×3/4×7″ UTW;23G×3/4×12″ UTW;21G×3/4×7″ UTW;21G×3/4×12″ UTW

by Guangzhou Improve Medical Instruments Co., Ltd

Identity

Trade Name
IMPROSAFE® ImPress Blood Collection Set EUDAMED
Device Name
Blood Collection Needle EUDAMED
Model / Reference
25G×3/4×7″ TW;25G×3/4×12″ TW;23G×3/4×7″ TW;23G×3/4×12″ TW;21G×3/4×7″ TW;21G×3/4×12″ TW;25G×3/4×7″ UTW;25G×3/4×12″ UTW;23G×3/4×7″ UTW;23G×3/4×12″ UTW;21G×3/4×7″ UTW;21G×3/4×12″ UTW EUDAMED
5991253002 EUDAMED

Identifiers

Primary DI / UDI-DI
06978565410548 EUDAMED
Basic UDI-DI
697856541001018YG 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® ImPress 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 39e3f4bb-dbda-457c-8c67-0648a9414bf3 61 fields · synced Jul 8, 2026