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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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CMV Brite Turbo kit — 1 UDI-DI variant, IVDD (IQ Products BV)

MD Atlas
IQ Products BV

Data from EUDAMED, last updated May 30, 2026

CMV Brite Turbo kit

B-08717953022301

1 UDI-DI variant

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]IVDD — Annex II List B

Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — Annex II List B
Manufacturer: IQ Products BV

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Device characteristics

Professional testingAnimal tissues / cells

Legacy certificates

Certificate number: 2114129CE01
Type: refdata.legacy.ivdd-certificate-type.iv-excluding-4-6
Notified body: DEKRA Certification B.V. (0344)
Validity: May 26, 2025

Identity & classification

Basic UDI-DI: B-08717953022301
Device name: CMV Brite Turbo kit
Device model: Kit
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — Annex II List B
Version date: Sep 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: IQ Products BV
SRN: NL-MF-000010812
Country: Netherlands
Email: orders@iqproducts.nl
Phone: +31 50 5757000

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J8MMW1D2HA9R1GS6J6XG0WP7

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

CMV Brite Turbo kit08717953022301