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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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ADL — 8 UDI-DI variants, MDR (Etac Supply Center AB)

MD Atlas
Etac Supply Center AB

Data from EUDAMED, last updated May 31, 2026

ADL

73204510354G

8 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: Etac Supply Center AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73204510354G
Device name: —
Device model: ADL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: Etac Supply Center AB
SRN: SE-MF-000001230
Country: Sweden
Email: info@etac.com
Phone: +46 371 587200

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01K6DA375DACBR4M9PZVK4DM1T

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

Aktiv07320450002441
Aktiv07320450002434
Aktiv07320450002458
Aktiv07320451357366
Aktiv07320451357373
Aktiv07320451357359
Aktiv07320450002465
Torkel07320450002014