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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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Organization name
UDI-DI code
Reference / catalog number

F004001008ACPI — Class I MDR by AUTO RIBEIRO LDA

MD Atlas
AUTO RIBEIRO LDA

EUDAMED last updated this device on Feb 25, 2025

F004001008ACPI

5600786656ARA1504A

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AUTO RIBEIRO LDA
UDI-DI code: 05600786656047
Reference / catalog number: F004001008ACPI

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View device family (Basic UDI)

Manufacturer information

Organization name: AUTO RIBEIRO LDA
SRN: PT-MF-000002814
Manufacturer status: Active

Related devices

F004006003ACP5600786656ARA150FB2On the market F004006002ACP5600786656ARA150FB2On the market F004006004ACP5600786656ARA150FB2On the market F004006001ACP5600786656ARA150FB2On the market F004001007ACPI5600786656ARA1504AOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Placed on the market in Portugal; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05600786656047
Basic UDI-DI: 5600786656ARA1504A
Reference / catalog number: F004001008ACPI
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V08050102SELF-LOADING STRETCHERS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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