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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

PP 020 — Class I MDR by abcMED spółka z…

MD Atlas
abcMED spółka z ograniczoną odpowiedzialnością

EUDAMED last updated this device on May 28, 2026

PP 020

590177933NARSAJ8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: abcMED spółka z ograniczoną odpowiedzialnością
UDI-DI code: 59017793301432
Reference / catalog number: PP 020

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Manufacturer information

Organization name: abcMED spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000034816
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement	Jan 18, 2011	Still on market

Device identification

Trade name: not provided
UDI-DI code: 59017793301432
Basic UDI-DI: 590177933NARSAJ8
Reference / catalog number: PP 020
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: Przewód PP 020 przeznaczony jest do połączenia pneumotachografu dPP oraz głowic BCTS lub NOX z modułem pomiarowym spirometru.
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

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12150199SPIROMETRY INSTRUMENTS - 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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Related devices

PS PNEUMO590177933DSSP3On the market KN 051590177933NADSAG2On the market DP 050590177933ADSAFPOn the market PP 015590177933NARSAJ8On the market PP 030590177933NARSAJ8On 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.