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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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Aprikos Medical AS

Certificate HU25/00000077

Rev. 1Issued
Valid until
Aug 7, 2030

Certificate HU25/00000077 is a valid Quality assurance issued to Aprikos Medical AS and registered in EUDAMED. Valid until August 7, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
HU25/00000077
Certificate type
Quality assurance
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
1639HU25/000000771

Validity

Issued
Aug 7, 2025
Valid from
Aug 7, 2025
Valid until
Aug 7, 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
No
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 I13

13 scopes

  • MDN1208, MDS1006
    Class I
  • Handles for scalpels
    Class I
  • Surgical knives
    Class I
  • Surgical scissors
    Class I
  • General surgery forceps
    Class I
  • Spreaders and retractors
    Class I
  • Fistula probes
    Class I
  • Bone Curettes
    Class I
  • Osteotomes
    Class I
  • Uterine curettes
    Class I
  • Bone rongeurs
    Class I
  • Needle Holders
    Class I
  • Haemostatic Forceps
    Class I

Documents

LanguagesEN

Manufacturer

Manufacturer
Aprikos Medical AS
Manufacturer SRN
NO-MF-000044411
Manufacturer country
Norway