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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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Pplus Skin Care Limited

Certificate M.2023.MDR.1029

Rev. 00Reissued
Valid until
Dec 1, 2028

Overview

Certificate number
M.2023.MDR.1029
Certificate type
Quality assurance
Certificate status
Reissued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
2696M.2023.MDR.102900

Validity

Issued
Dec 1, 2023
Valid from
Dec 1, 2023
Valid until
Dec 1, 2028

Manufacturer

Manufacturer
Pplus Skin Care Limited
Manufacturer SRN
GB-MF-000030057
Manufacturer country
United Kingdom

Notified body

Notified body
UDEM Adriatic d.o.o.
Notified body SRN
2696
Notified body country
Croatia

Covered devices

No specific devices are listed for this certificate.

Characteristics

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

History

Supersedes

  • M.2023.MDR.1029ReissuedApr 15, 2026 → Nov 30, 2028

Predecessor certificate not registered in EUDAMED.

Scope coverage

Class IIa1

1 scope

  • Sterile Ampoule
    Class IIa

Documents

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