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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

Lauma Medical — Class I MDR by Liepājas speciālās…

MD Atlas
Liepājas speciālās ekonomiskās zonas SIA Lauma Medical

EUDAMED last updated this device on Nov 10, 2025

Lauma Medical

4752231BANDAGESM3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Liepājas speciālās ekonomiskās zonas SIA Lauma Medical
UDI-DI code: 04752231000279
Reference / catalog number: 8 cm х 1.5 m

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View device family (Basic UDI)

Manufacturer information

Organization name: Liepājas speciālās ekonomiskās zonas SIA Lauma Medical
SRN: LV-MF-000021168
Manufacturer status: Active

Related devices

12 cm х 0.6 m4752231BANDAGESM3On the market 10 cm х 3.5 m4752231BANDAGESM3On the market Lauma Medical4752231BANDAGESM3On the market 10 cm х 5.0 m4752231BANDAGESM3On the market 10 cm х 2.0 m4752231BANDAGESM3On 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 Latvia; available across 3 countries total.

Country	On market since	Until
LatviaPrimary placement		Still on market
Germany		Still on market
Lithuania		Still on market

Device identification

Trade name: Lauma Medical
UDI-DI code: 04752231000279
Basic UDI-DI: 4752231BANDAGESM3
Reference / catalog number: 8 cm х 1.5 m
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: Can be used for the treatment and prevention of venous inflammation, before and after surgical procedures; for the prevention of post-traumatic complications and hematomas; for the fixation of prostheses during cosmetic surgery; as well as for the prevention and treatment of sports-related injuries.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 8 MU10
1.5 MU36

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04752231000279

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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.

M0304010103ELASTIC COMPRESSION BANDAGES, NON-ADHESIVE, HIGH EXTENSIBILITY (>140%)

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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