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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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Quantib Prostate — 4 UDI-DI variants, MDR (Quantib BV)

MD Atlas
Quantib BV

Data from EUDAMED, last updated May 30, 2026

Quantib Prostate

8719689791QPR1RH

4 UDI-DI variants

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

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

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 8719689791QPR1RH
Device name: Quantib Prostate
Device model: QPR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Dec 6, 2022

Manufacturer & authorised representative

Manufacturer

Name: Quantib BV
SRN: NL-MF-000027601
Country: Netherlands
Email: quality@quantib.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GKKQ0ADWYF763N5VQ999Q1GP

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

004-21008719689791209
004-31008719689791230
004-32008719689791278
004-33008719689791292