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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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SwimCount™ Harvester — 2 UDI-DI variants, MDR (MotilityCount ApS)

MD Atlas
MotilityCount ApS

Data from EUDAMED, last updated May 23, 2026

SwimCount™ Harvester

5745000420SWHARVESTERF6

2 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: MotilityCount ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5745000420SWHARVESTERF6
Device name: SwimCount™ Harvester
Device model: 1 mL and 3 mL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: MotilityCount ApS
SRN: DK-MF-000001507
Country: Denmark
Email: mct@motilitycount.com
Phone: +45 40 60 33 03

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KK133TFBF1GQVKG8FNPDHH3J

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

SwimCount™ Harvester05745000420049
SwimCount™ Harvester05745000420087