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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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M91227 — 2 UDI-DI variants, MDR (Medikro Oy)

MD Atlas
Medikro Oy

Data from EUDAMED, last updated May 23, 2026

M91227

6420099M91227B4

2 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: Medikro Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6420099M91227B4
Device name: —
Device model: M91227
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 18, 2021

Manufacturer & authorised representative

Manufacturer

Name: Medikro Oy
SRN: FI-MF-000011841
Country: Finland
Email: medikro@medikro.com
Phone: +358172833000

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FMS7FBCNTQ7RHG8C3JHDW5HK

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

Medikro Grip06420099001018
M91227-WA, ref 72147306420099001223