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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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Christeyns N.V.

Certificate TNP/MDR/0011/3870/2023

Rev. Ver. 02Supplemented
Valid until
Jan 25, 2028

Certificate TNP/MDR/0011/3870/2023 is a valid Quality assurance issued to Christeyns N.V. and registered in EUDAMED. Valid until January 25, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
TNP/MDR/0011/3870/2023
Certificate type
Quality assurance
Certificate status
Supplemented
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
2
Certificate ID
2274TNP/MDR/0011/3870/2023Ver. 02

Validity

Issued
May 5, 2025
Valid from
May 5, 2025
Valid until
Jan 25, 2028

Notified body

Notified body
TUV NORD Polska Sp. z o.o
Notified body SRN
2274
Notified body country
Poland

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile
No
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
No
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

Status changes

  • Supplemented

Supersedes

  • TNP/MDR/0011/3870/2023Quality assuranceIssuedApr 3, 2023 → Jan 25, 2028

Scope coverage

Class IIa10

10 scopes

  • Produkt na bazie kwasu nadoctowego do dezynfekcji nieinwazyjnych wyrobów medycznych / Peracetic acid based product for disinfecting non invasive medical devices
    Class IIa
  • Peracid Forte Combo
    Class IIa
  • Peracid Forte MDR
    Class IIa
  • Peracid Asepsis Combo
    Class IIa
  • Peracid Asepsis MDR
    Class IIa
  • Sanoxy Forte Combo
    Class IIa
  • Sanoxy Forte MDR
    Class IIa
  • Peracid Forte
    Class IIa
  • Peracid Asepsis
    Class IIa
  • Sanoxy Forte
    Class IIa

Manufacturer

Manufacturer
Christeyns N.V.
Manufacturer SRN
BE-MF-000003309
Manufacturer country
Belgium

Documents

LanguagesENPL