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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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Staining for histology — 7 UDI-DI variants, IVDR

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

Data from EUDAMED, last updated May 30, 2026

Staining for histology

080339762W0103010301AJ

7 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

Reagent

Identity & classification

Basic UDI-DI: 080339762W0103010301AJ
Device name: Staining for histology
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 4, 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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GH14JCXEVERN9R8PP6HC3DRA

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

05-12005E08033976232658
05-12005/L08033976232641
05-M1200508033976234881
05-M1200208033976234867
05-12002/L08033976232610
05-12002E08033976232627
04-09080508033976230999