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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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TOPRO Olympos ATR — 9 UDI-DI variants, MDR (Topro Industri AS)

MD Atlas
Topro Industri AS

Data from EUDAMED, last updated May 30, 2026

TOPRO Olympos ATR

705432OLY814334

9 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: Topro Industri AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 705432OLY814334
Device name: TOPRO Olympos ATR
Device model: TOPRO Olympos ATR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 30, 2022

Manufacturer & authorised representative

Manufacturer

Name: Topro Industri AS
SRN: NO-MF-000003447
Country: Norway
Email: kundeservice@topromobility.com
Phone: +4761 13 46 00

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01GBQ7EQEPXRAY6NJ6WH4PYMV5

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

12007007054321200703
12006007054321200604
12000007054321200000
12030107054321203018
12027007054321202707
12021007054321202103
12026007054321202608
12024007054321202400
12020007054321202004