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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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Disposable trimming board — 3 UDI-DI variants, IVDR

MD Atlas
Bio-Optica Milano S.p.A.

Data from EUDAMED, last updated May 30, 2026

Disposable trimming board

080339762W050190992J

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Bio-Optica Milano S.p.A.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 080339762W050190992J
Device name: Disposable trimming board
Device model: Trimming board
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: Bio-Optica Milano S.p.A.
SRN: IT-MF-000027525
Country: Italy
Email: info@bio-optica.it

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJ2FG1CJD0NQW095MZCB4SVP

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

DISPOSABLE TRIMMING BOARD08033976236540
DISPOSABLE TRIMMING BOARD08033976236557
DISPOSABLE TRIMMING BOARD08033976236564