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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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ABility Smart Extract — 2 UDI-DI variants, IVDR (APPOLON BIOTECK)

MD Atlas
APPOLON BIOTECK

Data from EUDAMED, last updated May 19, 2026

ABility Smart Extract

376032282APAN2234K

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: APPOLON BIOTECK

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 376032282APAN2234K
Device name: ABility Smart Extract
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Sep 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: APPOLON BIOTECK
SRN: FR-MF-000022234
Country: France
Email: contact@appolonbioteck.com
Phone: +33 4 37 57 00 54

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K4CZ3ATSV2KMAC17RX46BVBW

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

AB003003760322820133
AB003803760322820140