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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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Basic Unit Arthro — 14 UDI-DI variants, MDR

MD Atlas
M.I.S.S. Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Basic Unit Arthro

426072983PRPLH

14 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: M.I.S.S. Medizintechnik GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426072983PRPLH
Device name: Basic Unit Arthro
Device model: BU-A
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 16, 2023

Manufacturer & authorised representative

Manufacturer

Name: M.I.S.S. Medizintechnik GmbH
SRN: DE-MF-000020722
Country: Germany
Email: miss.gmbh@t-online.de
Phone: +49 3302 55030

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HCW4B79HK1Y551Q548ZKVHF1

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

71-435-0004260729830104
70-520-0004260729832023
UNT-16-00604260729830999
70520-0404260729832009
1143-204260729830975
tk39770-0004260729830791
EUP2-PU04260729830531
70-520-0604260729832016
CG-001-03004260729830586
70-520-0204260729832030
10840-00204260729830326
15-171604260729831194
BU-A04260729830005
EUP-PU-O04260729830562