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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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Poweradapter — 4 UDI-DI variants, MDR (A/S Aabentoft)

MD Atlas
A/S Aabentoft

Data from EUDAMED, last updated May 31, 2026

Poweradapter

5745000872HSPSU6E

4 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: A/S Aabentoft

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5745000872HSPSU6E
Device name: Poweradapter
Device model: Poweradapter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: A/S Aabentoft
SRN: DK-MF-000034597
Country: Denmark
Email: info@aabentoft.dk
Phone: +4586975300

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K6FWB9S46N9HNWZBQTTK9B7E

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

HPSUSB12072LX05745000872039
HPSUSB19072LX05745000872053
HPSUSB12072RN05745000872046
HPSUSB19072RN05745000872060