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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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20-2492317 Bibs 3 ply 38x68 cm — 2 UDI-DI variants, MDR (Ab Fatex Oy)

MD Atlas
Ab Fatex Oy

Data from EUDAMED, last updated May 23, 2026

20-2492317 Bibs 3 ply 38x68 cm

6430072530206Y

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Ab Fatex Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6430072530206Y
Device name: 20-2492317 Bibs 3 ply 38x68 cm
Device model: Bibs
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ab Fatex Oy
SRN: FI-MF-000041039
Country: Finland
Email: kevin.hogkvist@fatex.org
Phone: +358400269355

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01KQY3T4NXHJMSNJT72NKZ28HN

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

20-1492360 Bibs 2 ply 38x6806430072530077
20-2492317 Bibs 3 ply 38x68cm06430072530053