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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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ProMIL 245 — 5 UDI-DI variants, MDR (Frestems Oy)

MD Atlas
Frestems Oy

Data from EUDAMED, last updated May 23, 2026

ProMIL 245

6429810491F000102PP

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: Frestems Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6429810491F000102PP
Device name: ProMIL 245
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 18, 2022

Manufacturer & authorised representative

Manufacturer

Name: Frestems Oy
SRN: FI-MF-000001837
Country: Finland
Email: frestems@frestems.fi

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FW687121B712WWEDXHBTQQHS

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

ProMIL 24506429810491022
3546806429810491039
3578106429810491138
3517806429810491046
3578206429810491145