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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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Incontinence Pants — 2 UDI-DI variants, MDR (Intigena (Schweiz) AG)

MD Atlas
Intigena (Schweiz) AG

Data from EUDAMED, last updated May 23, 2026

Incontinence Pants

0761262100002QE

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Intigena (Schweiz) AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0761262100002QE
Device name: Incontinence Pants
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 31, 2022

Manufacturer & authorised representative

Manufacturer

Name: Intigena (Schweiz) AG
SRN: CH-MF-000019385
Country: Switzerland
Email: info@intigena.de

Authorised representative

Name: Intigena GmbH & Co. KG
SRN: DE-AR-000018822
Country: Germany

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FTQXYRGENFGQ4Z4JH0MSDR2R

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

0761262100025807612621000258
0761262100026507612621000265