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Lecigon PEG, ENFit

EUDAMED

Class IIb (EU MDR)

Ref 2120

by Innoventa Medica ApS

Identity

Device Name
Lecigon PEG, ENFit EUDAMED
Model / Reference
2120 EUDAMED

Identifiers

Primary DI / UDI-DI
05745000321049 EUDAMED
Basic UDI-DI
5745000321LecigonPEG4N EUDAMED
EMDN Code
G02020201 GASTROSTOMY, TUBES AND SETS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

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

Lecigon PEG, ENFit by Innoventa Medica ApS — Class IIb — 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
DK-MF-000013980

Sources (1)

  • EUDAMED b409a477-a0a6-42fe-b41c-3ca4a82affe3 61 fields · synced Jun 18, 2026