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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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FAT BINDER FORTE type 1 — 3 UDI-DI variants, MDR

MD Atlas
Omega Pharma International NV

Data from EUDAMED, last updated May 23, 2026

FAT BINDER FORTE type 1

5400951FBFORTIIBT1B3

3 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: Omega Pharma International NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5400951FBFORTIIBT1B3
Device name: FAT BINDER FORTE type 1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Omega Pharma International NV
SRN: BE-MF-000007210
Country: Belgium
Email: QAMeddev@perrigo.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K9A4BW9WJ6ZE83A0SBFGV97T

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

CT2808805400951001180
CT2808608470002055292
XLS Medical Pro 7 gélules05400951001104