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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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Automated Biochemistry Analyzer < 400… — 2 UDI-DI variants, IVDR

MD Atlas
BPC Biosed Srl

Data from EUDAMED, last updated May 30, 2026

Automated Biochemistry Analyzer < 400 tests/h

803367543GLOB2AF

2 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: BPC Biosed Srl

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 803367543GLOB2AF
Device name: Automated Biochemistry Analyzer < 400 tests/h
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: BPC Biosed Srl
SRN: IT-MF-000032961
Country: Italy
Email: info@bpcbiosed.it
Phone: +39 069073666

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JHN55STC16528DZC98VNGYW4

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

Automated Biochemistry Analyzer GLOBAL 24008033675432809
Automated Biochemistry Analyzer GLOBAL 72008033675433387