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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 ND — 3 UDI-DI variants, MDR (Quantib BV)

MD Atlas
Quantib BV

Data from EUDAMED, last updated May 30, 2026

Quantib ND

8719689791PGNDQM

3 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: Quantib BV

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Device characteristics

Active device

Legacy certificates

Certificate number: SCAR-13.2.2.1
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: Scarlet NB B.V. (3022)
Validity: May 26, 2026 → Aug 1, 2030

Identity & classification

Basic UDI-DI: 8719689791PGNDQM
Device name: Quantib ND
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 22, 2024

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HSJJM07Y1D10EN9F0GBKZNWM

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

000-15008719689791254
Quantib ND 1.608719689791032
Quantib ND 2.108719689791216