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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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Applicateur PS non sterile — 6 UDI-DI variants, MDR (Applimed SA)

MD Atlas
Applimed SA

Data from EUDAMED, last updated May 23, 2026

Applicateur PS non sterile

0764017844NAppPSc58

6 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: Applimed SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0764017844NAppPSc58
Device name: Applicateur PS non sterile
Device model: 1202180
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Applimed SA
SRN: CH-MF-000046641
Country: Switzerland
Email: info@applimed.ch
Phone: +41 21 948 92 74

Authorised representative

Name: Dansu A/S
SRN: DK-AR-000046254
Country: Denmark
Phone: +45 48181274

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K56BK6EM27WDEADFBZYFAA2Q

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

120218007640178446366
121124907640178445932
121124807640178434585
121124707640178434578
121124607640178441422
120221807640178442993