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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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SOLOASSIST II — 20 UDI-DI variants, MDR (AKTORmed GmbH)

MD Atlas
AKTORmed GmbH

Data from EUDAMED, last updated May 23, 2026

SOLOASSIST II

4260463840018T

20 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: AKTORmed GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4260463840018T
Device name: SOLOASSIST II
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 19, 2021

Manufacturer & authorised representative

Manufacturer

Name: AKTORmed GmbH
SRN: DE-MF-000006136
Country: Germany
Email: info@aktormed.com
Phone: +49 9401 93 20 110

Variants by status

UDI-DI variants

20 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FJC6XA7KPNHHRXG78230FW3S

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

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21248004260463844801
21249904260463844993
14136304260463843637
22259004260463845907
21248204260463844825
17203504260463840353
21251804260463845181
14136404260463843644
18222004260463842203
17209904260463840995
19228204260463842821
17205404260463840544
14133904260463843392
16177304260463847734
16177404260463847741
14136504260463843651
12087404260463848748
14136204260463843620
17189504260463848953