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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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AsthmaTuner — 3 UDI-DI variants, MDR (MediTuner AB)

MD Atlas
MediTuner AB

Data from EUDAMED, last updated May 31, 2026

AsthmaTuner

735014837ATSN

3 UDI-DI variants

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 735014837ATSN
Device name: AsthmaTuner
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: MediTuner AB
SRN: SE-MF-000028534
Country: Sweden
Email: info@medituner.se

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP865EX0VQ1CANEV5X6KG6VT

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

AsthmaTuner07350148370033
6.1.0.007350148370019
6.0.0.007350148370002