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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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Nitrilové rukavice — 124 UDI-DI variants, MDR (Espeon, s.r.o.)

MD Atlas
Espeon, s.r.o.

Data from EUDAMED, last updated May 23, 2026

Nitrilové rukavice

859417720NITRILUS

124 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: Espeon, s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859417720NITRILUS
Device name: Nitrilové rukavice
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: Espeon, s.r.o.
SRN: CZ-MF-000049569
Country: Czechia
Email: maka@espeon.cz
Phone: +420739349829

Variants by status

UDI-DI variants

124 UDI-DI variants

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Applied filters

basicUdiUlid01KCHNBKRN9S2F17PGHKGWNP4P

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

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10015608594177201534
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10018308594177201800
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10018608594177201824
10013408594177201312
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10018208594177201794
10018008594177201770
10010008594177200971
10010208594177200995
10009908594177200964
10019208594177201893

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