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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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AIRKit Plus — 3 UDI-DI variants, MDR (Pikdare S.p.A.)

MD Atlas
Pikdare S.p.A.

Data from EUDAMED, last updated May 31, 2026

AIRKit Plus

805809038301000JS

3 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: Pikdare S.p.A.

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 805809038301000JS
Device name: AIRKit Plus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Pikdare S.p.A.
SRN: IT-MF-000010069
Country: Italy
Email: istituzionale@pec.pikdare.it
Phone: +39031729111

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQVMNGXV07Z6PRQ733VYYZVS

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

5803830100000008058090048558
5803830200000008058090048565
5803830300000008058090048572