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GLICOFIL·LAC fast

EUDAMED

Class III (EU MDR)

Ref FW500LR

by Assut Europe Spa

Identity

Trade Name
GLICOFIL·LAC fast EUDAMED
Device Name
GLICOFIL LAC FAST EUDAMED
Model / Reference
FW500LR EUDAMED

Identifiers

Primary DI / UDI-DI
38033439428179 EUDAMED
Basic UDI-DI
8033439GLICOFLACFAST7N EUDAMED
Direct Marketing DI
38033439428179 EUDAMED
EMDN Code
H010101020201,H010101020202,H010101020203 EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

GLICOFIL·LAC fast by Assut Europe Spa — Class III — 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

Manufacturer
Assut Europe Spa
EUDAMED SRN
IT-MF-000018178

Sources (1)

  • EUDAMED 9beddcf0-6619-4a1a-b3b0-e03dc8fbde54 61 fields · synced Aug 1, 2026