Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

41305408592602249670
41305508592602249687
41305608592602249694
41305708592602249700
41320808592602253530
41320908592602253547
41321008592602253554
41321108592602253561
41305808592602249717
41305908592602249724
41306008592602249731
41306108592602249748
41321208592602253578
41321308592602253585
41321408592602253592
41321508592602253608
41317508592602200619
41321608592602253615
41317908592602249434
41317808592602249427
41322708592602254124
41322608592602254117
41323108592602254162
41323008592602254155
41309208592602249410

1 2 3 4 5