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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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Shin poong Pharm Co.,Ltd.

Certificate 2025-MDR/QS-048

Rev. 00Issued
Valid until
Sep 27, 2027

Certificate 2025-MDR/QS-048 is a valid Quality management system issued to Shin poong Pharm Co.,Ltd. and registered in EUDAMED. Valid until September 27, 2027. View the full certificate record on MD Atlas.

Overview

Certificate number
2025-MDR/QS-048
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
22652025-MDR/QS-04800

Validity

Issued
Sep 24, 2025
Valid from
Sep 24, 2025
Valid until
Sep 27, 2027

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
Yes
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
—
QMS/MOS type
Basic UDI-DI data only

History

No status changes or preceding certificates are recorded.

Scope coverage

Class III2

2 scopes

  • Prefilled syringes with sterile physiological solution
    Class III
  • DEVICE
    Class III

Documents

LanguagesEN

Manufacturer

Manufacturer
Shin poong Pharm Co.,Ltd.
Manufacturer SRN
KR-MF-000009206
Manufacturer country
South Korea

Covered devices

  • HYALFORTE INJECTIONClass III
    880610380010CB