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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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OPRA Implant System - Accessories — 10 UDI-DI variants, MDR

MD Atlas
Integrum AB

Data from EUDAMED, last updated May 31, 2026

OPRA Implant System - Accessories

73401521accessoriesopra73

10 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: Integrum AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73401521accessoriesopra73
Device name: OPRA Implant System - Accessories
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Integrum AB
SRN: SE-MF-000026900
Country: Sweden
Email: quality@integrum.se
Phone: +46317601060

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K97H5GKY2HVJZAAS3NR7998P

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

147507340152101198
147907340152101204
IBK000307340152101242
167107340152101655
271007340152102393
271907340152102409
IBK004307340152101273
IBK004207340152101266
IBK004107340152101341
129007340152101259