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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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Inpeco Total Laboratory Automation — 3 UDI-DI variants, IVDR

MD Atlas
Inpeco SA

Data from EUDAMED, last updated May 23, 2026

Inpeco Total Laboratory Automation

764017234TLAKW

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: Inpeco SA

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 764017234TLAKW
Device name: Inpeco Total Laboratory Automation
Device model: TLA
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 23, 2023

Manufacturer & authorised representative

Manufacturer

Name: Inpeco SA
SRN: CH-MF-000017833
Country: Switzerland
Email: Regulatory.Affairs@inpeco.com

Authorised representative

Name: QbD RepS BV
SRN: BE-AR-000000040
Country: Belgium
Phone: +32 3 844 45 01

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01H13ZJW9272DZS4Y4Z7N48VEV

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

AP207640172342008
FLX07640172340004
FXX07640172344002