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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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Vendari DARIFLEX — 10 UDI-DI variants, MDR (Calvo Izquierdo S.L.)

MD Atlas
Calvo Izquierdo S.L.

Data from EUDAMED, last updated May 23, 2026

Vendari DARIFLEX

84306551058XER

10 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: Calvo Izquierdo S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84306551058XER
Device name: Vendari DARIFLEX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Calvo Izquierdo S.L.
SRN: ES-MF-000001063
Country: Spain
Email: admin@calvoizquierdo.es
Phone: +32 962349094

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KD7PNFQDSCVPZEZFCHXH0R59

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

1056308430655105638
1058308430655105836
1058408430655105843
1056408430655105645
1058008430655105805
1056008430655105607
1058108430655105812
1056108430655105614
1058208430655105829
1056208430655105621