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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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DANFLOW — 8 UDI-DI variants, MDR

MD Atlas
MEDKONSULT medical technology s.r.o.

Data from EUDAMED, last updated May 23, 2026

DANFLOW

859421157DANFLOWPS

8 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: MEDKONSULT medical technology s.r.o.

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: 2022-MDR/QS-001/A
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Jul 29, 2022 → Mar 21, 2027

Identity & classification

Basic UDI-DI: 859421157DANFLOWPS
Device name: DANFLOW
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: MEDKONSULT medical technology s.r.o.
SRN: CZ-MF-000016193
Country: Czechia
Email: regulatory@mmtsystems.com
Phone: +420 581 113 030

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G38GY8EVP08B1RJ95MMGZJ04

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

MU100208594211570015
MU110208594211570022
MU100108594211570039
MU110108594211570046
FU120108594211570114
FU120008594211570107
FU110008594211570121
FU110108594211570138