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High Flow Tubing

EUDAMED

Class I (EU MDR)

Ref HFT-110-E

by MIVI Neuroscience

Identity

Device Name
High Flow Tubing EUDAMED
Model / Reference
HFT-110-E EUDAMED

Identifiers

Primary DI / UDI-DI
B293HFT110E0 EUDAMED
Basic UDI-DI
B-B293HFT110E0 EUDAMED
EMDN Code
G020399 EVACUATION TUBES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

High Flow Tubing by MIVI Neuroscience — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
MIVI Neuroscience
EUDAMED SRN
US-MF-000020746
Authorised Representative
ICON (LR) Limited IE-AR-000006507

Sources (1)

  • EUDAMED 2f8a38cc-7ad2-46d2-ac7b-f0ffcdc16cd2 61 fields · synced Jun 18, 2026