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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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Ionization Chamber series MDD — 1 UDI-DI variant, MDD

MD Atlas
Varex Imaging Group Nederland B.V.

Data from EUDAMED, last updated May 30, 2026

Ionization Chamber series MDD

B-08718755002683

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Varex Imaging Group Nederland B.V.

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Device characteristics

Active device

Legacy certificates

Certificate number: BE19/819943480
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: SGS Belgium NV (1639)
Validity: May 24, 2024

Identity & classification

Basic UDI-DI: B-08718755002683
Device name: Ionization Chamber series MDD
Device model: ICX2122B
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Varex Imaging Group Nederland B.V.
SRN: NL-MF-000002153
Country: Netherlands
Email: eudamed.nl@vareximaging.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KRGK8W6XMBYVARYHG8DA4JYF

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

Varex Imaging08718755002683