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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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Inflation kits — 8 UDI-DI variants, MDR (CARDIVAIS S.A.)

MD Atlas
CARDIVAIS S.A.

Data from EUDAMED, last updated May 23, 2026

Inflation kits

842965905794LW

8 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: CARDIVAIS S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 842965905794LW
Device name: Inflation kits
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: CARDIVAIS S.A.
SRN: ES-MF-000017980
Country: Spain
Email: cardiva@cardivais.com
Phone: +34 952334350

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JMCDK8TGRF47HCR9BXPHSSFE

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

4K110408429659016750
4K110308429659016743
4K140108429659035348
4K120208429659021150
4K110208429659019652
4K120108429659024311
4K120308429659024564
4K110108429659024328