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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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Promilless — 5 UDI-DI variants, MDR (Testi Technologies Oy)

MD Atlas
Testi Technologies Oy

Data from EUDAMED, last updated May 23, 2026

Promilless

643005980AT1ES

5 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: Testi Technologies Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 643005980AT1ES
Device name: Promilless
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 4, 2022

Manufacturer & authorised representative

Manufacturer

Name: Testi Technologies Oy
SRN: FI-MF-000020503
Country: Finland
Email: info@promilless.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FXA9PWJNTJRS5JEWWKEJE78N

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

PR 2024-0706430059800599
Promilless 0,5 single06430059800452
Promilless 0,5‰06430059800308
306430059800490
Promilless ZERO06430059800223