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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 0101 Uniwersalny pas brzuszny z… — 7 UDI-DI variants, MDR

MD Atlas
SIGVARIS SPÓŁKA AKCYJNA

Data from EUDAMED, last updated May 30, 2026

PT 0101 Uniwersalny pas brzuszny z zapięciem "30"

5906699PT0101YM

7 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: 5906699PT0101YM
Device name: PT 0101 Uniwersalny pas brzuszny z zapięciem "30"
Device model: PT 0101 Uniwersalny pas brzuszny z zapięciem "30"
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 13, 2022

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

7 UDI-DI variants

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basicUdiUlid01G7VBKBHKA3E1GF5KP437JK3P

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

101XL05906699000053
101S05906699000022
101XXXL05906699014159
101M05906699000039
101L05906699000046
101XS05906699000015
101XXL05906699000060