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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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Optik Sutter Brillenwerk 3D-Fassungen… — 13 UDI-DI variants, MDR

MD Atlas
Optik Sutter e.U.

Data from EUDAMED, last updated May 23, 2026

Optik Sutter Brillenwerk 3D-Fassungen (BWSO01)

912014381BWOS014W

13 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: Optik Sutter e.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 912014381BWOS014W
Device name: Optik Sutter Brillenwerk 3D-Fassungen (BWSO01)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Optik Sutter e.U.
SRN: AT-MF-000052724
Country: Austria
Email: post@optiksutter.at
Phone: +43557233363

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMQ97Q7GPNAC8P7FVZNRA4GY

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

BW01-M-5209120143810081
BW01-M-5009120143810067
BW01-M-4809120143810043
BW01-M-5709120143810135
BW01-M-5809120143810142
BW01-M-4709120143810036
BW01-M-5609120143810128
BW01-M-5109120143810074
BW01-M-5509120143810111
BW01-M-4909120143810050
BW01-M-5309120143810098
BW01-M-4609120143810029
BW01-M-5409120143810104