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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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Applicateurs bois non sterile — 10 UDI-DI variants, MDR (Applimed SA)

MD Atlas
Applimed SA

Data from EUDAMED, last updated May 23, 2026

Applicateurs bois non sterile

0764017844NAppWoo98

10 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: 0764017844NAppWoo98
Device name: Applicateurs bois non sterile
Device model: 1001200
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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K453WB1AFN31XCZ794PXWMX7

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

100120207640178442962
102129207640178441859
101112407640178442504
100147207640178441378
100120807640178434646
102124507640178441408
100123007640178441361
100120007640178445390
102127507640178441903
102246707640178444782