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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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Dr. Müller Pharma s.r.o.

Certificate 2023-MDR/QS-034/C

Rev. 3Supplemented
Valid until
Oct 20, 2028

Certificate 2023-MDR/QS-034/C is a valid Quality management system issued to Dr. Müller Pharma s.r.o. and registered in EUDAMED. Valid until October 20, 2028. View the full certificate record on MD Atlas.

Overview

Certificate number
2023-MDR/QS-034/C
Certificate type
Quality management system
Certificate status
Supplemented
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
3
Certificate ID
22652023-MDR/QS-034/C3

Validity

Issued
Mar 23, 2026
Valid from
Mar 23, 2026
Valid until
Oct 20, 2028

Notified body

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

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
No
QMS/MOS type
Basic UDI-DI data only

History

Status changes

  • Supplemented

Supersedes

  • 2023-MDR/QS-034/AQuality management systemSupplementedDec 20, 2024 → Oct 20, 2028

Scope coverage

Class IIa2

2 scopes

  • Oral administration preparations not included in other classes
    Class IIa
  • DEVICE
    Class IIa

Manufacturer

Manufacturer
Dr. Müller Pharma s.r.o.
Manufacturer SRN
CZ-MF-000000005
Manufacturer country
Czechia

Covered devices

  • PastillesClass IIa
    85956104SLHR

Documents

LanguagesCSEN