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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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CAD. TRANSF. C610 — 8 UDI-DI variants, MDR (AUTO RIBEIRO LDA)

MD Atlas
AUTO RIBEIRO LDA

Data from EUDAMED, last updated May 30, 2026

CAD. TRANSF. C610

5600786656ARC61055

8 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: 5600786656ARC61055
Device name: —
Device model: CAD. TRANSF. C610
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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JE8QYDVFNZ1KNZYN4SNPVF5M

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

F007001005VRM05600786656689
F007001006AZL05600786656696
F007001005PRT05600786656665
F007001006VRM05600786656719
F007001006PRT05600786656702
F007001005VRD05600786656672
F007001005AMR05600786656153
F007001005AZL05600786656658