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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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Flexo — 1 UDI-DI variant, MDR (Lopital Nederland B.V.)

MD Atlas
Lopital Nederland B.V.

Data from EUDAMED, last updated May 30, 2026

Flexo

872025610303551005199GC

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Lopital Nederland B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 872025610303551005199GC
Device name: Flexo
Device model: 51005199
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: Lopital Nederland B.V.
SRN: NL-MF-000004372
Country: Netherlands
Email: dennis.van.eijkeren@lopital.nl
Phone: +31135239300

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KQRZX2S77CQX9DMNY8Z2T7SZ

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

5100519908720256103035