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Sheath

EUDAMED

Class A (EU MDR)

Ref Sheath-XN 10LModel Sheath-Sys,Sheath-Ruby,Sheath-XN

by B&E Bio-Technology Co., Ltd.

Identity

Device Name
Sheath EUDAMED
Model / Reference
Sheath-Sys,Sheath-Ruby,Sheath-XN EUDAMED
Sheath-XN 10L EUDAMED

Identifiers

Primary DI / UDI-DI
06972337857845 EUDAMED
Basic UDI-DI
697233785Sheath022NM EUDAMED
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) 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

Yes

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

Sheath by B&E Bio-Technology 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-000023256
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED a3733f70-43b9-42d2-a7e2-9329f348d63b 61 fields · synced Jun 18, 2026