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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 products — 7 UDI-DI variants, MDR

MD Atlas
Medicline društvo s ograničenom odgovornošću za trgovinu i proizvodnju

Data from EUDAMED, last updated May 24, 2026

Incontinence products

385889598INCO0001H9

7 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: Medicline društvo s ograničenom odgovornošću za trgovinu i proizvodnju

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 385889598INCO0001H9
Device name: Incontinence products
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Medicline društvo s ograničenom odgovornošću za trgovinu i proizvodnju
SRN: HR-MF-000048512
Country: Croatia
Email: lucija.hren@medicline.hr

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K5X9N6Q9QNM9QEE4ACYD7X0B

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

603003858895980009
604003858895980016
17717703858895980122
703003858895980023
804003858895980054
704003858895980030
705003858895980047