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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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Pryžové obinadlo škrticí — 2 UDI-DI variants, MDR (ŠTĚPAŘ s.r.o.)

MD Atlas
ŠTĚPAŘ s.r.o.

Data from EUDAMED, last updated May 23, 2026

Pryžové obinadlo škrticí

85951302102845C

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: ŠTĚPAŘ s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85951302102845C
Device name: Pryžové obinadlo škrticí
Device model: Pryžové obinadlo škrticí 25 x 750 mm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: ŠTĚPAŘ s.r.o.
SRN: CZ-MF-000023035
Country: Czechia
Email: stepar@stepar.cz
Phone: +420461724460

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K6MYW7HT06GP9GTJPCPQ2DW8

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

SKR2508595130200502
SKR6008595130200434