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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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mikrozid sensitive — 15 UDI-DI variants, MDR (Schülke & Mayr GmbH)

MD Atlas
Schülke & Mayr GmbH

Data from EUDAMED, last updated May 23, 2026

mikrozid sensitive

4032651BSC00000021A2

15 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: Schülke & Mayr GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4032651BSC00000021A2
Device name: mikrozid sensitive
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Schülke & Mayr GmbH
SRN: DE-MF-000005701
Country: Germany
Email: info@schuelke.com

Variants by status

UDI-DI variants

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KM4TQ9Y7DT21541HMDV5T4F7

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

7000311104032651981007
7000311204032651981021
7000402304032651986422
7000313404032651981298
7000313604032651981335
7000313504032651981311
7000310204032651980864
7000314504032651981397
7000310904032651980987
7000310304032651980888
7000310104032651980840
7000310404032651980901
7000314404032651981373
7000310804032651980963
7000367004032651985494