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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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HomeAccess — 17 UDI-DI variants, MDR (Trident Industri AB)

MD Atlas
Trident Industri AB

Data from EUDAMED, last updated May 31, 2026

HomeAccess

73400609HomeAccessYQ

17 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: Trident Industri AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73400609HomeAccessYQ
Device name: —
Device model: HomeAccess
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: Trident Industri AB
SRN: SE-MF-000044390
Country: Sweden
Email: info@trident.se
Phone: +46431449500

Variants by status

UDI-DI variants

17 UDI-DI variants

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Applied filters

basicUdiUlid01KBF9W66QCTSS8VNNYY4WNVEV

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

20067107340060900012
20143107340060900029
20066807340060900036
20143407340060900043
20047307340060900050
20143707340060900067
20115807340060900074
20144007340060900081
20115707340060900098
20144307340060900104
20115607340060900111
20144607340060900128
20149307340060900166
20103307340060900135
20108207340060900159
20106107340060900142
20070707340060900173