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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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SynSwab Collector — 1 UDI-DI variant, IVDR (MolGen BV)

MD Atlas
MolGen BV

Data from EUDAMED, last updated May 30, 2026

SynSwab Collector

87202998305RCPT7B

1 UDI-DI variant

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: MolGen BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87202998305RCPT7B
Device name: SynSwab Collector
Device model: 08720299830530
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 16, 2022

Manufacturer & authorised representative

Manufacturer

Name: MolGen BV
SRN: NL-MF-000022886
Country: Netherlands
Email: info@molgen.com
Phone: +3185 200 7431

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01GJ0JE534F9SV864X7WGK10W3

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

SynSwab Collector08720299830530