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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 EXTRA — 9 UDI-DI variants, MDR (Calvo Izquierdo S.L.)

MD Atlas
Calvo Izquierdo S.L.

Data from EUDAMED, last updated May 23, 2026

Vendari EXTRA

84306551010XDD

9 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: 84306551010XDD
Device name: Vendari EXTRA
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

9 UDI-DI variants

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Applied filters

basicUdiUlid01KD7P91S7MQFYEM4JBJCKK9W5

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

SANOCREPE 10cm x 4m08430655900301
SANOCREPE 5cm x 4m08430655900288
SANOCREPE 7cm x 4m08430655900295
1010108430655000018
1010208430655000025
1010508430655000056
1010608430655000063
1010408430655000049
1010308430655000032