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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 — 3 UDI-DI variants, MDR (PF mobility ApS)

MD Atlas
PF mobility ApS

Data from EUDAMED, last updated May 23, 2026

Adaptive cycle

5745000343SBS6A

3 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5745000343SBS6A
Device name: Adaptive cycle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 11, 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KKE6R8KEQB04SNB6RWEJPQ89

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

500040005745000343164
500043005745000343171
500010005745000343157