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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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Przewód pneumotachografu dPP — 3 UDI-DI variants, MDR

MD Atlas
abcMED spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

Przewód pneumotachografu dPP

590177933NARSAJ8

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: abcMED spółka z ograniczoną odpowiedzialnością

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590177933NARSAJ8
Device name: Przewód pneumotachografu dPP
Device model: Przewód pneumotachografu dPP 1.5 m
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: abcMED spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000034816
Country: Poland
Email: biuro@abcmed.pl
Phone: +48126368954

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSQAC02T72SR8CE65SGFJK8E

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

PP 01559017793301296
PP 02059017793301432
PP 03059017793301678