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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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Serum protein separation reagent kit — 2 UDI-DI variants, IVDR

MD Atlas
FUTURLAB S.R.L.

Data from EUDAMED, last updated May 30, 2026

Serum protein separation reagent kit

805889430FENZLV

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: FUTURLAB S.R.L.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 805889430FENZLV
Device name: Serum protein separation reagent kit
Device model: SP KIT
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: FUTURLAB S.R.L.
SRN: IT-MF-000046539
Country: Italy
Email: franco.milia@futurlab.it
Phone: +390498843461

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSMS3CG85EX02RXTKY3DR3MR

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

FE051NZ-5KIT80588943001804
FE051NZ-680588943001972