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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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Įtvarinė sistema čiurnos sąnariui — 2 UDI-DI variants, MDR

MD Atlas
UAB Pirmas žingsnis

Data from EUDAMED, last updated May 30, 2026

Įtvarinė sistema čiurnos sąnariui

477905276PKA311HG

2 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: UAB Pirmas žingsnis

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 477905276PKA311HG
Device name: Įtvarinė sistema čiurnos sąnariui
Device model: PKA311
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 25, 2023

Manufacturer & authorised representative

Manufacturer

Name: UAB Pirmas žingsnis
SRN: LT-MF-000004764
Country: Lithuania
Email: info@pirmaszingsnis.lt
Phone: +37037409280

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H8P03889HH3121BH6CVTWBJ2

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

TD/12404779052761950
TD/12404779052761967