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IMPROMINI® Capillary Blood Collection Tube

EUDAMED

Class A (EU MDR)

Ref 5656605;Model Lithium Heparin Tube;Sodium Heparin Tube;Glucose Tube;EDTA.K2 Tube;EDTA.K3 Tube;Gel& EDTA.K2 Tube;Gel & Lithium Heparin Tube;Gel& Sodium Heparin Tube

by Guangzhou Improve Medical Instruments Co., Ltd

Identity

Trade Name
IMPROMINI® Capillary Blood Collection Tube EUDAMED
Device Name
Capillary Blood Collection Tube EUDAMED
Model / Reference
Lithium Heparin Tube;Sodium Heparin Tube;Glucose Tube;EDTA.K2 Tube;EDTA.K3 Tube;Gel& EDTA.K2 Tube;Gel & Lithium Heparin Tube;Gel& Sodium Heparin Tube EUDAMED
5656605; EUDAMED

Identifiers

Primary DI / UDI-DI
06978565410739 EUDAMED
Basic UDI-DI
697448183008003WD EUDAMED
EMDN Code
W0501010203 BLOOD COLLECTION, CAPILLARY TUBES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Cyprus EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

IMPROMINI® Capillary Blood Collection Tube by Guangzhou Improve Medical Instruments Co., Ltd. — Class A — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000006536
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED ce24e95b-0510-4f00-aa56-57151f2ae284 61 fields · synced Jun 19, 2026