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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 DARIGRIP — 33 UDI-DI variants, MDR (Calvo Izquierdo S.L.)

MD Atlas
Calvo Izquierdo S.L.

Data from EUDAMED, last updated May 23, 2026

Vendari DARIGRIP

84306551050XDZ

33 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: 84306551050XDZ
Device name: Vendari DARIGRIP
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

33 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KD7Q8VE8DNY5EYSEPANGEGV0

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

91051108430655910515
1051108430655105119
1050208430655105027
91051208430655910522
1051208430655105126
91051308430655910539
1050408430655105041
91051408430655910546

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