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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 AF forte — 6 UDI-DI variants, MDR (Schülke & Mayr GmbH)

MD Atlas
Schülke & Mayr GmbH

Data from EUDAMED, last updated May 23, 2026

gigasept AF forte

4032651BSC00000035AD

6 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: 4032651BSC00000035AD
Device name: gigasept AF forte
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 6, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KK1HND15SNMCN2M0ZJ37G1QX

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

7000357004032651984756
7000356904032651984732
7000341204032651984336
7000357204032651984787
7000341304032651984350
7000357304032651984794