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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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Barcode Set — 1 UDI-DI variant, IVDR (4bases SA)

MD Atlas
4bases SA

Data from EUDAMED, last updated May 31, 2026

Barcode Set

764041338600X3N

1 UDI-DI variant

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: 4bases SA

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 764041338600X3N
Device name: Barcode Set
Device model: Barcode Set
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: 4bases SA
SRN: CH-MF-000042125
Country: Switzerland
Email: martina.fabi@4bases.ch
Phone: +41799258443

Authorised representative

Name: 4bases Italia srl
SRN: IT-AR-000041271
Country: Italy

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSQMS8QG70K4PX7GC9XC7E7A

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

600176404133800590