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A150

by Auto Ribeiro Lda Portugal EUDAMED

Ref F004004006ACPIModel CHARRIOT A150 EMDN V08050102

Overview

Explore the A150 medical device, a Class I instrument designed for various applications. Learn about its features, specifications, and testing, as well as its compliance status and FDA registration.

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5600786656ARA1504A Basic UDI-DIDate4 Dec 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Model / Reference
CHARRIOT A150, F004004006ACPI
Primary DI / UDI-DI
05600786656481
Basic UDI-DI
5600786656ARA1504A
Direct Marketing DI
05600786656481
EMDN Code
V08050102 Self-loading stretchers
Device Class
Class I
Market of Registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000002814

Other devices from Auto Ribeiro Lda

See all devices from Auto Ribeiro Lda →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 04a59155-62c3-45d3-b821-6fbf655a280b 61 fields · synced 23 Oct 2026