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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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Samyang Biopharm Corporation

Certificate 2024-MDR/QS-068/B

Rev. 02Supplemented
Valid until
Dec 12, 2029

Certificate 2024-MDR/QS-068/B is a valid Quality management system issued to Samyang Biopharm Corporation and registered in EUDAMED. Valid until December 12, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
2024-MDR/QS-068/B
Certificate type
Quality management system
Certificate status
Supplemented
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
3
Certificate ID
22652024-MDR/QS-068/B02

Validity

Issued
Feb 18, 2026
Valid from
Feb 18, 2026
Valid until
Dec 12, 2029

Notified body

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

Characteristics

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

History

Status changes

  • Supplemented

Supersedes

  • 2024-MDR/QS-068/AQuality management systemAmendedJan 5, 2026 → Dec 12, 2029

Scope coverage

Class III2

2 scopes

  • Poliglecaprone and derivatives monofilament with needle for tissue traction (‘barbed’) Absorbable Knotless Wound Closure Device
    Class III
  • DEVICE
    Class III

Documents

LanguagesEN

Manufacturer

Manufacturer
Samyang Biopharm Corporation
Manufacturer SRN
KR-MF-000037085
Manufacturer country
South Korea

Covered devices

  • Absorbable Knotless Wound Closure DeviceClass III
    880936647KF01LQ