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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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Inion Instruments — 57 UDI-DI variants, MDR (Inion Oy)

MD Atlas
Inion Oy

Data from EUDAMED, last updated May 23, 2026

Inion Instruments

6438408INION-IR-INSTRUM9T

57 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: Inion Oy

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 6438408INION-IR-INSTRUM9T
Device name: Inion Instruments
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: Inion Oy
SRN: FI-MF-000000646
Country: Finland
Email: info@inion.com

Variants by status

UDI-DI variants

57 UDI-DI variants

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Applied filters

basicUdiUlid01JC5E0KWN5H3W1G4N8D4FG2WY

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

No registered UDI-DI variants for this device family.