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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

REF532047 — Class I MDR by Liepājas Speciālās…

MD Atlas
Liepājas Speciālās ekonomiskās zonas SIA NordePlast

EUDAMED last updated this device on Mar 24, 2026

REF532047

475102853REF532047K5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Liepājas Speciālās ekonomiskās zonas SIA NordePlast
UDI-DI code: 04751028532047
Reference / catalog number: REF532047

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View device family (Basic UDI)

Manufacturer information

Organization name: Liepājas Speciālās ekonomiskās zonas SIA NordePlast
SRN: LV-MF-000026735
Manufacturer status: Active

Related devices

REF531309475102853REF531309K5On the market REF534423475102853REF534423KROn the market REF532153475102853REF532153K5On the market REF532016475102853REF532016JSOn the market REF532313475102853REF532313K3On 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Latvia; available across 1 country total.

Placed on the market in Latvia; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04751028532047
Basic UDI-DI: 475102853REF532047K5
Reference / catalog number: REF532047
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: 72 x 19 mm; 10 pcs.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04751028532047

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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.

M0599MEDICAL PLASTERS - 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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