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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

APS912952 — Class I MDR by NTRADE Sp. z o.o.

MD Atlas
NTRADE Sp. z o.o.

EUDAMED last updated this device on Jul 7, 2025

APS912952

5908243486PLOPSTPL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NTRADE Sp. z o.o.
UDI-DI code: 05904204912952
Reference / catalog number: APS912952

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View device family (Basic UDI)

Manufacturer information

Organization name: NTRADE Sp. z o.o.
SRN: PL-MF-000019255
Manufacturer status: Active

Related devices

LPO4867025908243486PLOPSTPLOn the market APO4864745908243486PLOPSTPLOn the market APO9126485908243486PLOPSTPLOn the market APO4864505908243486PLOPSTPLOn the market APO6032075908243486PLOPSTPLOn 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 Poland; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05904204912952
Basic UDI-DI: 5908243486PLOPSTPL
Reference / catalog number: APS912952
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: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05904204912952

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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.

M04010199ADHESIVE DRESSINGS, WITH ABSORBENT PAD - 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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