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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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ALDS — 4 UDI-DI variants, MDR (Lothar Medtec GmbH)

MD Atlas
Lothar Medtec GmbH

Data from EUDAMED, last updated May 23, 2026

ALDS

42700010235ALDS-ACCS8P

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Lothar Medtec GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 42700010235ALDS-ACCS8P
Device name: ALDS
Device model: ALDS Hardware Accessories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Lothar Medtec GmbH
SRN: DE-MF-000007469
Country: Germany
Email: info@lothar-medtec.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KB5D6NJE1S1XK3MBXC18VQ5B

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

ALDM FENO04262466450102
ALDM SPIRO04262466450058
ALDS04262466450041
ALDS PRO04262466450096