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Test Tube

EUDAMED

Class A (EU MDR)

Ref 5mlΦ13*75psModel Plastic Test Tube 3mlΦ12*60ps,5mlΦ12*75pp,5mlΦ13*75pp,5mlΦ12*75ps,5mlΦ13*75ps,7mlΦ12*100ps,7mlΦ13*100ps,10mlΦ15*100pp,10mlΦ16*100pp,10mlΦ16*102ps

by Yiwu Eason Medical Devices Co., Ltd.

Identity

Device Name
Test Tube EUDAMED
Model / Reference
Plastic Test Tube 3mlΦ12*60ps,5mlΦ12*75pp,5mlΦ13*75pp,5mlΦ12*75ps,5mlΦ13*75ps,7mlΦ12*100ps,7mlΦ13*100ps,10mlΦ15*100pp,10mlΦ16*100pp,10mlΦ16*102ps EUDAMED
5mlΦ13*75ps EUDAMED

Identifiers

Primary DI / UDI-DI
06977346241012 EUDAMED
Basic UDI-DI
697734624TT01RE EUDAMED
EMDN Code
W0599 IVD GENERAL USE CONSUMABLE DEVICES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

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

Test Tube by Yiwu Eason Medical Devices Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000041286
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 6a30fc65-990c-4c08-afce-fcb744165661 61 fields · synced Jun 19, 2026