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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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Ceruloplasmina/ceruloplasmin — 1 UDI-DI variant, IVDD

MD Atlas
GIESSE DIAGNOSTICS SRL

Data from EUDAMED, last updated May 30, 2026

Ceruloplasmina/ceruloplasmin

B-08053172971885

1 UDI-DI variant

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]IVDD — General

Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Manufacturer: GIESSE DIAGNOSTICS SRL

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: B-08053172971885
Device name: Ceruloplasmina/ceruloplasmin
Device model: 6705
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Version date: Mar 31, 2026

Manufacturer & authorised representative

Manufacturer

Name: GIESSE DIAGNOSTICS SRL
SRN: IT-MF-000039031
Country: Italy
Email: info@giessediagnostics.com
Phone: +39 0774 051100

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KN23PS8N1C5Y6JY0W0FFATMP

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

Ceruloplasmin08053172971885