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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

940.570 — Class I MDR by IMO - Indústrias…

MD Atlas
IMO - Indústrias Metalúrgicas, S.A.

EUDAMED last updated this device on Sep 13, 2023

940.570

5600717213IMO3U

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: IMO - Indústrias Metalúrgicas, S.A.
UDI-DI code: 05600717213103
Reference / catalog number: 940.570

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View device family (Basic UDI)

Manufacturer information

Organization name: IMO - Indústrias Metalúrgicas, S.A.
SRN: PT-MF-000006644
Manufacturer status: Active

Related devices

940.5315600717213IMO3UOn the market 590.165600717213ZEROG2QOn the market 591.1525600717213FINEUZOn the market 591.0525600717213FINEUZOn the market 940.532.25600717213IMO3UOn 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: 05600717213103
Basic UDI-DI: 5600717213IMO3U
Reference / catalog number: 940.570
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

UDI-DI DataMatrix

Encoded

(01)05600717213103

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

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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