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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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Adapter — 6 UDI-DI variants, MDR (Sedana Medical Limited)

MD Atlas
Sedana Medical Limited

Data from EUDAMED, last updated May 24, 2026

Adapter

539153029026002FG

6 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: Sedana Medical Limited

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 539153029026002FG
Device name: Adapter
Device model: Reusable Abbvie QuikFil® Adapter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Sedana Medical Limited
SRN: IE-MF-000001734
Country: Ireland
Email: prrc@sedanamedical.com
Phone: +353 (0)87 359 3312

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K8B4FX5KGWF4RJBMXBCB5GN0

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

2604205391530290104
2604405391530290418
102604505391530290722
2606405391530290098
102604905391530290470
2604805391530290296