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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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OPT GENERIC ACCESSORY — 2 UDI-DI variants, MDR (OPT SURGISYSTEMS)

MD Atlas
OPT SURGISYSTEMS

Data from EUDAMED, last updated May 31, 2026

OPT GENERIC ACCESSORY

8050539130006W3

2 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: OPT SURGISYSTEMS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8050539130006W3
Device name: OPT GENERIC ACCESSORY
Device model: OPT GENERIC ACCESSORY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: OPT SURGISYSTEMS
SRN: IT-MF-000009326
Country: Italy
Email: regolatory@opt-ita.com
Phone: +39 0464 834336

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KBJ8862G961XN6X8K0PWS9HR

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

990100108050539137557
901000008050539137595