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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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OBVAZ HYDROFILNÍ PLETENÝ, nesterilní — 8 UDI-DI variants, MDR

MD Atlas
STERIWUND spol. s r.o.

Data from EUDAMED, last updated May 23, 2026

OBVAZ HYDROFILNÍ PLETENÝ, nesterilní

85951541004VC

8 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: STERIWUND spol. s r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85951541004VC
Device name: OBVAZ HYDROFILNÍ PLETENÝ, nesterilní
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: STERIWUND spol. s r.o.
SRN: CZ-MF-000036963
Country: Czechia
Email: steriwund@steriwund.cz
Phone: +420 733 110 862

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMJ2SN29Q45HN7YKKK6XBRV6

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

017008595154102134
017208595154102400
017408595154102394
101308595154113789
017308595154102257
012408595154111785
013008595154111792
014308595154111808