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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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CHARRIOT A150F — 4 UDI-DI variants, MDR (AUTO RIBEIRO LDA)

MD Atlas
AUTO RIBEIRO LDA

Data from EUDAMED, last updated May 30, 2026

CHARRIOT A150F

5600786656ARA150FB2

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: AUTO RIBEIRO LDA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5600786656ARA150FB2
Device name: —
Device model: CHARRIOT A150F
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: AUTO RIBEIRO LDA
SRN: PT-MF-000002814
Country: Portugal
Email: geral@autoribeiro.com
Phone: +351 227157100

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JE8DDY29GTQJX9Y1XHFG06K5

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

F004006004ACP05600786656450
F004006001ACP05600786656092
F004006003ACP05600786656443
F004006002ACP05600786656436