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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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Amiko_on_Ellipta — 3 UDI-DI variants, MDR (AMIKO SRL)

MD Atlas
AMIKO SRL

Data from EUDAMED, last updated May 30, 2026

Amiko_on_Ellipta

805572743RESPIROSENSUS

3 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: AMIKO SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805572743RESPIROSENSUS
Device name: Amiko_on_Ellipta
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 9, 2023

Manufacturer & authorised representative

Manufacturer

Name: AMIKO SRL
SRN: IT-MF-000010697
Country: Italy
Email: info@amiko.io
Phone: +390284084092

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01H2G3Q3NA9EYNEJS5NZCVZ7ZF

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

Amiko_on_Aerosol08055727430106
Amiko_on_Ellipta08055727430007
Amiko_on_Nexthaler08055727430021