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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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H&O Equipments nv/sa

Certificate BE25/00000310

Rev. 1Issued
Valid until
Dec 8, 2030

Certificate BE25/00000310 is a valid Quality management system issued to H&O Equipments nv/sa and registered in EUDAMED. Valid until December 8, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
BE25/00000310
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
1639BE25/000003101

Validity

Issued
Dec 8, 2025
Valid from
Dec 8, 2025
Valid until
Dec 8, 2030

Notified body

Notified body
SGS Belgium NV
Notified body SRN
1639
Notified body country
Belgium

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
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

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa3

3 scopes

  • MDA0303
    Class IIa
  • CryoPen/Freezpen: CryoPen/Freezpen
    Class IIa
  • CryoPen/Freezpen: N2O Gas Cartridge
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
H&O Equipments nv/sa
Manufacturer SRN
BE-MF-000000992
Manufacturer country
Belgium