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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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ClickIt ER instruments — 1 UDI-DI variant, MDR (Mikai s.p.a.)

MD Atlas
Mikai s.p.a.

Data from EUDAMED, last updated May 30, 2026

ClickIt ER instruments

8055731430ERINSTRUMENTSA4

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Mikai s.p.a.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8055731430ERINSTRUMENTSA4
Device name: —
Device model: ClickIt ER instruments
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: Mikai s.p.a.
SRN: IT-MF-000030732
Country: Italy
Email: mikai@mikai.it
Phone: +39 010 30801

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JQV859PP6RBMFQ1WEYWPR37Z

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

5000124M08055400671734