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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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Adaptive cycle — 20 UDI-DI variants, MDR (PF mobility ApS)

MD Atlas
PF mobility ApS

Data from EUDAMED, last updated May 23, 2026

Adaptive cycle

5745000343DP20T6

20 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: PF mobility ApS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5745000343DP20T6
Device name: Adaptive cycle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: PF mobility ApS
SRN: DK-MF-000018768
Country: Denmark
Email: info@pfmobility.dk
Phone: +4599920600

Variants by status

UDI-DI variants

20 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMMKKC3E0X42XAN6YPTTCSZC

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

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500055005745000343072
500056005745000343270
500057005745000343263
50029505745000343058
500029005745000343065
500029905745000343249
500029705745000343256
510012005745000343140
510013005745000343133
510014005745000343393
510015005745000343386
500038005745000343102
500038505745000343096
500039205745000343287
500039005745000343294
500030505745000343126
500030605745000343119
500030705745000343317
500030805745000343300