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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Lecigon PEG, ENFit — 2 UDI-DI variants, MDR (Innoventa Medica ApS)

MD Atlas
Innoventa Medica ApS

Data from EUDAMED, last updated May 31, 2026

Lecigon PEG, ENFit

5745000321LecigonPEG4N

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Innoventa Medica ApS

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Device characteristics

Implantable

Legacy certificates

Certificate number: 68620146168
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: Intertek Medical Notified Body AB (2862)
Validity: Mar 21, 2023 → Mar 20, 2028

Identity & classification

Basic UDI-DI: 5745000321LecigonPEG4N
Device name: Lecigon PEG, ENFit
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: Innoventa Medica ApS
SRN: DK-MF-000013980
Country: Denmark
Email: info@innoventamedica.com
Phone: +45 26221962

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H7CHEQ223J6YN8R1S27QKPWE

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

212005745000321049
211505745000321032