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LiquiPhil™

EUDAMED

Class I (EU MDR)

Ref TLP250Model LiquiPhil™

by Phantom Laboratory

Identity

Trade Name
LiquiPhil™ EUDAMED
Device Name
TLP250 EUDAMED
Model / Reference
LiquiPhil™ EUDAMED
TLP250 EUDAMED

Identifiers

Primary DI / UDI-DI
D-TLP250HU EUDAMED
Basic UDI-DI
B-TLP250HU EUDAMED
EMDN Code
Z119080 VARIOUS BIOIMAGING AND RADIOTHERAPY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

No

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

LiquiPhil™ by Phantom Laboratory — 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
Phantom Laboratory
EUDAMED SRN
US-MF-000027490
Authorised Representative
Hoff & Lowendahl AB SE-AR-000001888

Sources (1)

  • EUDAMED 03d36d19-cbc7-487b-b498-36ffb07b79fb 61 fields · synced Jun 19, 2026