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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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Mesa Italia S.r.l.

Certificate 0425-MDR-030016-00

Rev. 00Issued
Valid until
Jan 31, 2028

Overview

Certificate number
0425-MDR-030016-00
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
04250425-MDR-030016-0000

Validity

Issued
Feb 1, 2023
Valid from
Feb 1, 2023
Valid until
Jan 31, 2028

Manufacturer

Manufacturer
Mesa Italia S.r.l.
Manufacturer SRN
IT-MF-000029407
Manufacturer country
Italy

Notified body

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

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
Basic UDI-DI data only

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa5

5 scopes

  • Leghe metalliche a base di cobalto, ferro, nichel e titanio per protesi scheletrate, ponti e corone, ceramiche e saldatura. Cobalt, iron, nickel and titanium metal alloys for partial dentures, bridges and crowns, ceramics and weldings.
    Class IIa
  • DEVICE
    Class IIa
  • DEVICE
    Class IIa
  • DEVICE
    Class IIa
  • DEVICE
    Class IIa

Documents

LanguagesENIT

Covered devices

  • 80506122000000000000001TWClass IIa
    80506122000000000000001TW
  • 80506122000000000000000TUClass IIa
    80506122000000000000000TU
  • 80506122000000000000002TYClass IIa
    80506122000000000000002TY
  • 80506122000000000000011TZClass IIa
    80506122000000000000011TZ