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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

8434048536580 — Class I MDR by LABORATOIRE POLIDIS

MD Atlas
LABORATOIRE POLIDIS

EUDAMED last updated this device on Jul 30, 2025

8434048536580

3664538ADGL04PRRC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATOIRE POLIDIS
UDI-DI code: 08434048536580
Reference / catalog number: 8434048536580

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Manufacturer information

Organization name: LABORATOIRE POLIDIS
SRN: FR-MF-000004550
Manufacturer status: Active

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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.

Market distribution

Primary placement in Portugal; available across 2 countries total.

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

Device identification

Trade name: not provided
UDI-DI code: 08434048536580
Basic UDI-DI: 3664538ADGL04PRRC
Reference / catalog number: 8434048536580
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: 75 MU03

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification