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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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ProSense Antihalkstrumpor — 1 UDI-DI variant, MDR (Tjugohundra18 AB)

MD Atlas
Tjugohundra18 AB

Data from EUDAMED, last updated May 30, 2026

ProSense Antihalkstrumpor

734018574404201G6

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Tjugohundra18 AB

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UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KNFDQJ3EX1894DR6841E700Z

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

4404207340185700153

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 734018574404201G6
Device name: ProSense Antihalkstrumpor
Device model: 44042
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Tjugohundra18 AB
SRN: SE-MF-000003776
Country: Sweden
Email: info@prosense.nu
Phone: +46 723090600

Variants by status