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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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Scavenging Accessory — 2 UDI-DI variants, MDR (Sedana Medical Limited)

MD Atlas
Sedana Medical Limited

Data from EUDAMED, last updated May 24, 2026

Scavenging Accessory

539153029026004FL

2 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: 539153029026004FL
Device name: Scavenging Accessory
Device model: Scavenging Tube
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 6, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01K9C6DRPPGTG63CHTTFDMCBVD

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

102606305391530290746
102605705391530290777