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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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Calibration Tube — 5 UDI-DI variants, MDR (Bariatric Solutions GmbH)

MD Atlas
Bariatric Solutions GmbH

Data from EUDAMED, last updated May 23, 2026

Calibration Tube

0426044057TUBESV7

5 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: Bariatric Solutions GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0426044057TUBESV7
Device name: Calibration Tube
Device model: TUBE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: Bariatric Solutions GmbH
SRN: CH-MF-000011469
Country: Switzerland
Email: info@bariatric-solutions.com
Phone: +41527416500

Authorised representative

Name: Bariatric Solutions Europe BV
SRN: NL-AR-000010444
Country: Netherlands
Phone: +31 76 204 31 54

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01GS80DJNEG7KR8W300TSHNNP2

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

Calibration TUBE32W04260440573007
Calibration TUBE34R04260440573014
Calibration TUBE36B04260440573021
Calibration TUBE38G04260440573038
Calibration TUBE40Y04260440573045