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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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PT 0345 Temblak kończyny górnej YOUNG — 6 UDI-DI variants, MDR

MD Atlas
SIGVARIS SPÓŁKA AKCYJNA

Data from EUDAMED, last updated May 31, 2026

PT 0345 Temblak kończyny górnej YOUNG

5906699PT0345ZK

6 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: SIGVARIS SPÓŁKA AKCYJNA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5906699PT0345ZK
Device name: PT 0345 Temblak kończyny górnej YOUNG
Device model: PT 0345 Temblak kończyny górnej YOUNG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: SIGVARIS SPÓŁKA AKCYJNA
SRN: PL-MF-000004824
Country: Poland
Email: sekretariat@sigvaris.com
Phone: +48 61 43 88 200

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KCGN6A0XCWPPF659BXB6YJ3H

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

PT 0345 Arm sling YOUNG05906699086330
PT 0345 Arm sling YOUNG05906699086309
PT 0345 Arm sling YOUNG05906699086286
PT 0345 Arm sling YOUNG05906699086323
PT 0345 Arm sling YOUNG05906699086316
PT 0345 Arm sling YOUNG05906699086293