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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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InKina — 3 UDI-DI variants, MDR

MD Atlas
S.A.L.F. S.p.A. Laboratorio Farmacologico

Data from EUDAMED, last updated May 30, 2026

InKina

805274210InKInaP5

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: S.A.L.F. S.p.A. Laboratorio Farmacologico

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805274210InKInaP5
Device name: InKina
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: S.A.L.F. S.p.A. Laboratorio Farmacologico
SRN: IT-MF-000010720
Country: Italy
Email: regulatory@salfspa.it
Phone: +39035940097

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GERP0D9D6CZ16HRJYG67B21K

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

InKina08052742102780
InKina08052742102766
InKina08052742102773