Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Master Polymer Plus Detection System… — 4 UDI-DI variants, IVDR

MD Atlas
VITRO, S.A.

Data from EUDAMED, last updated May 23, 2026

Master Polymer Plus Detection System (Phosphatase) (Incl. AP Chromogen)

8435421200453XZ

4 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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 8435421200453XZ
Device name: Master Polymer Plus Detection System (Phosphatase) (Incl. AP Chromogen)
Device model: MAD-000230QK
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 19, 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

4 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01G0EKK66Y1G9FW40PV0V6V435

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-000230QK08435421215092
MAD-000230QK-10/N08435421230651
MAD-000230QK-1008435421215108
MAD-000230QK/N08435421215191