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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

603683 — Class IIb MDR by LABORATOIRES URGO

MD Atlas
LABORATOIRES URGO

EUDAMED last updated this device on May 13, 2026

603683

354689UM01034T

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATOIRES URGO
UDI-DI code: 03546890045389
Reference / catalog number: 603683

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Manufacturer information

Organization name: LABORATOIRES URGO
SRN: FR-MF-000002559
Manufacturer status: Active

Related devices

Bande adhésive élastique354689UM00204NOn the market 605881354689UM008058On the market 605880354689UM008058On the market 605847354689UM00685JOn the market 605968354689UM00785MOn the market

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03546890045389
Basic UDI-DI: 354689UM01034T
Reference / catalog number: 603683
Issuing entity: GS1

Classification

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

Device details

Quantity: 20
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 10cm x 10cm

EMDN nomenclature code(s)

M04040602POLYURETHANE DRESSINGS, COMBINED WITH OTHER SUBSTANCES

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

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.