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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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Osmometer — 8 UDI-DI variants, IVDR (Axel Löser Messtechnik)

MD Atlas
Axel Löser Messtechnik

Data from EUDAMED, last updated May 23, 2026

Osmometer

PP12562OSMOMETER42

8 UDI-DI variants

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: Axel Löser Messtechnik

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: PP12562OSMOMETER42
Device name: Osmometer
Issuing agency: IFA
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: Axel Löser Messtechnik
SRN: DE-MF-000023401
Country: Germany
Email: info@loeser-osmometer.de

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G395D59PX6VTGMJCZP4BWV25

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

TYP16.C1312562TYP16.C072
TYP7M1312562TYP7M056
TYP16.CM1312562TYP16.CM091
TYP7iM1312562TYP7IM063
TYP71312562TYP7074
TYP7i1312562TYP7I004
TYP16M1312562TYP16M035
TYP161312562TYP16073