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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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IS-10 — 2 UDI-DI variants, MDR (M.I.S.S. Medizintechnik GmbH)

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

Data from EUDAMED, last updated May 23, 2026

IS-10

426072983LAPJA

2 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 device

Identity & classification

Basic UDI-DI: 426072983LAPJA
Device name: IS-10
Device model: IS-10
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 22, 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

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GW49BVSHWBNJV3DYSWSNC2AC

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

750-506004260729830272
IS10-N-G210N00004260729830128