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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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octenisept gel — 9 UDI-DI variants, MDR (Schülke & Mayr GmbH)

MD Atlas
Schülke & Mayr GmbH

Data from EUDAMED, last updated May 23, 2026

octenisept gel

4032651BSC00000032A7

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Schülke & Mayr GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4032651BSC00000032A7
Device name: octenisept gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 13, 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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Applied filters

basicUdiUlid01KKJT44PEWKHQK2MT1YHSWZHJ

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

7000297604032651980284
7000342404032651984527
12160504032651216055
7000337304032651983988
7000302104032651980444
12160704032651216079
12161004032651216109
12161104032651216116
12160604032651216062