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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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Selectra ProM — 7 UDI-DI variants, IVDR (VitalScientific B.V. )

MD Atlas
VitalScientific B.V.

Data from EUDAMED, last updated May 31, 2026

Selectra ProM

37017008ProM-SeriesSL

7 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: VitalScientific B.V.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 37017008ProM-SeriesSL
Device name: Selectra ProM
Device model: 6003-404
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: VitalScientific B.V.
SRN: NL-MF-000021018
Country: Netherlands
Email: a.intveld@vitalscientific.com
Phone: +31(0)313 430555

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KG2B21B3J9TSPR7XZ4F0MH2M

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

6003-40703701700864813
Selectra ProM03701700864837
6003-40503701700864790
6003-40603701700864806
6003-43903701700864820
Selectra ProM03701700860396
6003-40403701700864783