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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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IASO-LITE-BF2 — 3 UDI-DI variants, IVDR (A.S.T. s.r.l.)

MD Atlas
A.S.T. s.r.l.

Data from EUDAMED, last updated May 30, 2026

IASO-LITE-BF2

805384180IASO-LITE-BF2FB

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: A.S.T. s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805384180IASO-LITE-BF2FB
Device name: IASO-LITE-BF2
Device model: IASO-LITE
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jun 9, 2023

Manufacturer & authorised representative

Manufacturer

Name: A.S.T. s.r.l.
SRN: IT-MF-000029421
Country: Italy
Email: info@asteng.it
Phone: +390350791020

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01H2G5TNKKCD0ECT66GEYH2KT4

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

0658-IASO-LITE-BF280538418000658
IASO-LITE-BF380538418000726
IASO-LITE-BF480538418000894