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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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  • MD Atlas
  • Documents

Shin poong Pharm Co.,Ltd.

Certificate 2022-MDR/TD-023/A

Rev. 01Issued
Valid until
Sep 27, 2027

Certificate 2022-MDR/TD-023/A is a valid Technical documentation 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
2022-MDR/TD-023/A
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
22652022-MDR/TD-023/A01

Validity

Issued
Oct 6, 2023
Valid from
Oct 6, 2023
Valid until
Sep 27, 2027

Notified body

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

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

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

  • Device
    880610380654DV

Documents

LanguagesEN

Manufacturer

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

Covered devices

  • 880610380654DVClass III
    880610380654DV

Linked SSCPs

  • SSCP SP-SSCP-001