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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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BEZNOSKA, s.r.o.

Certificate 2023-MDR/TD-005/A

Rev. 01Supplemented
Valid until
May 12, 2028

Overview

Certificate number
2023-MDR/TD-005/A
Certificate type
Technical documentation
Certificate status
Supplemented
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
22652023-MDR/TD-005/A01

Validity

Issued
Mar 5, 2026
Valid from
Mar 5, 2026
Valid until
May 12, 2028

Manufacturer

Manufacturer
BEZNOSKA, s.r.o.
Manufacturer SRN
CZ-MF-000000543
Manufacturer country
Czechia

Notified body

Notified body
3EC International a.s.
Notified body SRN
2265
Notified body country
Slovakia

Covered devices

  • REPLACEMENT OF PART OF THE UPPER LIMB - Replacement of Trapeziometacarpal JointClass III
    859260207001FZ

Characteristics

Sterile
—
Human tissues
—
Animal tissues
—
In vitro diagnostics
—
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
No
Intended medical purpose
—
SPP applicable
—
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Others

History

Status changes

  • Supplemented

Supersedes

  • 2023-MDR/TD-005IssuedMay 11, 2023 → May 11, 2028

Predecessor certificate not registered in EUDAMED.

Scope coverage

Unspecified1

1 scope

  • REPLACEMENT OF PART OF THE UPPER LIMB - Replacement of Trapeziometacarpal Joint
    859260207001FZ

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