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Sclerotherapy set

EUDAMED

Class I (EU MDR)

Ref 02987202D121Ref 02987202D120

by Pentaferte Italia Srl

Identity

Trade Name
Sclerotherapy set EUDAMED
Sclerotherapy set (in individual case) EUDAMED
Device Name
EASYFOAM EUDAMED
Model / Reference
02987202D121 EUDAMED
02987202D120 EUDAMED

Identifiers

Primary DI / UDI-DI
08015262000103 EUDAMED
08015262000097 EUDAMED
Basic UDI-DI
801526210752 EUDAMED
EMDN Code
A019007 SCLEROTHERAPY NEEDLES AND KITS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sclerotherapy set by Pentaferte Italia Srl — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IT-MF-000040982

Sources (2)

  • EUDAMED bac92c26-5153-405f-9fe1-e35db7094db7 61 fields · synced Jul 22, 2026
  • EUDAMED 6cfcf4e3-4687-48e2-af51-877a9fdccd85 61 fields · synced May 18, 2026