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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

704.4915 — Class I MDR by Produtos Médicos…

MD Atlas
Produtos Médicos Hospitalares, SA

EUDAMED last updated this device on Apr 27, 2026

704.4915

560771670492

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Produtos Médicos Hospitalares, SA
UDI-DI code: 05607716049153
Reference / catalog number: 704.4915

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View device family (Basic UDI)

Manufacturer information

Organization name: Produtos Médicos Hospitalares, SA
SRN: PT-MF-000007631
Manufacturer status: Active

Related devices

702.488256077167028WOn the market 702.489056077167028WOn the market 206.496756077162007ZOn the market 206.441556077162007ZOn the market 206.436156077162007ZOn 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

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Portugal; available across 3 countries total.

Country	On market since	Until
PortugalPrimary placement		Still on market
Germany		Still on market
Spain		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05607716049153
Basic UDI-DI: 560771670492
Reference / catalog number: 704.4915
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: SACO FLEXÍVEL 1/1,5/2L S/ORIFÍCIO-TANDEM, S/ENTI-ESPUMA
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.

A060399FLUID COLLECTION BAGS AND SYSTEMS - OTHER

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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