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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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PIETRASANTA PHARMA S.p.A.

Certificate 0425-MDR-030169-01

Rev. 01Issued
Valid until
Jan 11, 2031

Overview

Certificate number
0425-MDR-030169-01
Certificate type
Quality assurance
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
04250425-MDR-030169-0101

Validity

Issued
Jan 12, 2026
Valid from
Jan 12, 2026
Valid until
Jan 11, 2031

Notified body

Notified body
ICIM S.P.A.
Notified body SRN
0425
Notified body country
Italy

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
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 I10

10 scopes

  • DISPOSITIVI MEDICI PER LA COMPRESSIONE DELLA FERITA E/O PER L'ASSORBIMENTO DEGLI ESSUDATI DISPOSITIVO MEDICO PER SUTURE CUTANEE / MEDICAL DEVICES FOR WOUND COMPRESSION AND/OR FOR ABSORPTION OF EXUDATES MEDICAL DEVICE FOR SKIN SUTURES
    Class I
  • MASTER-AID DERMATESS
    Class I
  • MASTER-AID DERMATESS COTONE
    Class I
  • MASTER-AID OPTOMED SIMPLEX
    Class I
  • MASTER-AID OPTOMED
    Class I
  • MASTER-AID DROP
    Class I
  • MASTER-AID STERIBLOCK DIA
    Class I
  • MASTER-AID STERIBLOCK DIA BEIGE
    Class I
  • MASTER-AID STERIBLOCK VENO
    Class I
  • MASTER-AID STERIGRAP
    Class I

Documents

LanguagesENIT

Manufacturer

Manufacturer
PIETRASANTA PHARMA S.p.A.
Manufacturer SRN
IT-MF-000018175
Manufacturer country
Italy