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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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VAX-ID® 2200 — 6 UDI-DI variants, MDR (Idevax BV)

MD Atlas
Idevax BV

Data from EUDAMED, last updated May 23, 2026

VAX-ID® 2200

5430003573000022000000UC

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Idevax BV

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 5430003573000022000000UC
Device name: VAX-ID® 2200
Device model: VAX-ID® 2200
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Idevax BV
SRN: BE-MF-000028217
Country: Belgium
Email: info@idevax.com
Phone: +32 3550 0031

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K1TEMM1HC631WQ18NHZ8R348

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

VAX-ID® 2200 27G sterile05430003573020
VAX-ID® 2200 27G to be sterilized05430003573044
VAX-ID® 2200 30G sterile05430003573013
VAX-ID® 2200 30G to be sterilized05430003573051
VAX-ID® 2200 32G sterile05430003573006
VAX-ID® 2200 32G to be sterilized05430003573037