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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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Swiss-Trac — 4 UDI-DI variants, MDR (Atec Ingenieurbüro AG)

MD Atlas
Atec Ingenieurbüro AG

Data from EUDAMED, last updated May 23, 2026

Swiss-Trac

7649991158Swiss-Trac3N

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: Atec Ingenieurbüro AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7649991158Swiss-Trac3N
Device name: Swiss-Trac
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Atec Ingenieurbüro AG
SRN: CH-MF-000027577
Country: Switzerland
Email: info@swisstrac.ch
Phone: +41418548020

Authorised representative

Name: be-on-market GmbH
SRN: DE-AR-000006148
Country: Germany

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JRRARMQ2A03KQPC1D8V06BXB

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

SWT-107649991158012
SWT-1HD07649991158043
SWT-1S07649991158036
SWT-207649991158029