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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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gigasept Instru AF — 9 UDI-DI variants, MDR (Schülke & Mayr GmbH)

MD Atlas
Schülke & Mayr GmbH

Data from EUDAMED, last updated May 23, 2026

gigasept Instru AF

4032651BSC00000037AH

9 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: 4032651BSC00000037AH
Device name: gigasept Instru AF
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 9, 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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNRFDP8ZD67GRM5NWN9TZCCG

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

10742704032651074273
gigasept Instru AF04032651074235
10741304032651074136
10742804032651074280
10742404032651074242
10742604032651074266
10741204032651074129
10742504032651074259
10741104032651074112