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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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REPLACEMENT OF PART OF THE UPPER LIMB… — 111 UDI-DI variants, MDR

MD Atlas
BEZNOSKA, s.r.o.

Data from EUDAMED, last updated May 23, 2026

REPLACEMENT OF PART OF THE UPPER LIMB - Replacement of Trapeziometacarpal Joint

859260207001FZ

111 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class III

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: BEZNOSKA, s.r.o.

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Device characteristics

Implantable

Legacy certificates

Certificate number: 2023-MDR/QS-005/A
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Mar 5, 2026 → May 12, 2028

Certificate number: 2023-MDR/TD-005/A
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: 3EC International a.s. (2265)
Validity: Mar 5, 2026 → May 12, 2028

Identity & classification

Basic UDI-DI: 859260207001FZ
Device name: REPLACEMENT OF PART OF THE UPPER LIMB - Replacement of Trapeziometacarpal Joint
Device model: ELIS, Type: T
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: BEZNOSKA, s.r.o.
SRN: CZ-MF-000000543
Country: Czechia
Email: petr.mracno@beznoska.cz
Phone: +420 312 811 266

Variants by status

UDI-DI variants

111 UDI-DI variants

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Applied filters

basicUdiUlid01KNKP30P24YEZSN8YYKZ3HPD3

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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41317208592602200602
41317108592602200596
41302108592602249519
41302608592602249564
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41302808592602249588
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41300408592602145453
41301008592602253325
41300508592602242503
41300808592602253332
41301108592602200466

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