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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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MID-LASER — 6 UDI-DI variants, MDR (Spectro Analytic Irradia AB)

MD Atlas
Spectro Analytic Irradia AB

Data from EUDAMED, last updated May 30, 2026

MID-LASER

735014983MID-LASER6A

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Spectro Analytic Irradia AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 735014983MID-LASER6A
Device name: MID-LASER
Device model: MID-LASER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Spectro Analytic Irradia AB
SRN: SE-MF-000030783
Country: Sweden
Email: info@irradia.se

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KK13H1FZQ70WFZWNZ822YV7F

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

MID-LASER07350149830048
Prob 635-107350149830093
Prob 635-407350149830086
Prob 904-107350149830079
Prob 904-1207350149830055
Prob 904-407350149830062