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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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Master Polymer Plus Detection System… — 3 UDI-DI variants, IVDR

MD Atlas
VITRO, S.A.

Data from EUDAMED, last updated May 23, 2026

Master Polymer Plus Detection System (Peroxidase)

8435421200455Y5

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: VITRO, S.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 8435421200455Y5
Device name: Master Polymer Plus Detection System (Peroxidase)
Device model: MAD-000237QP-100/V
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 9, 2022

Manufacturer & authorised representative

Manufacturer

Name: VITRO, S.A.
SRN: ES-MF-000001498
Country: Spain
Email: regulatory@vitro.bio
Phone: +34 954 933 200

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G1FXZY8V49Q1QECA31ZWZES2

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

MAD-000237QKVSBC08435421290938
MAD-000237QP-100/V08435421229020
MAD-000237QKVS08435421281479