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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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PROTHEOS INDUSTRIE

Certificate 39976

Rev. 2Issued
Valid until
Aug 27, 2029

Certificate 39976 is a valid Technical documentation issued to PROTHEOS INDUSTRIE and registered in EUDAMED. Valid until August 27, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
39976
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0459399762

Validity

Issued
Mar 27, 2026
Valid from
Mar 27, 2026
Valid until
Aug 27, 2029

Notified body

Notified body
GMED SAS
Notified body SRN
0459
Notified body country
France

Characteristics

Sterile
—
Human tissues
—
Animal tissues
—
In vitro diagnostics
—
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
No
Intended medical purpose
—
SPP applicable
—
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified4

4 scopes

  • XLMOB cementless acetabular shell
    ++EPRS15040000BUH
  • XLMOB cemented acetabular shell
    ++EPRS15050000BUW
  • XLMOB conventional PE acetabular insert
    ++EPRS16080000BWQ
  • XLMOB crosslinked polyethylene acetabular insert
    ++EPRS16180000BX9

Manufacturer

Manufacturer
PROTHEOS INDUSTRIE
Manufacturer SRN
FR-MF-000000150
Manufacturer country
France

Covered devices

  • XLMOB cementless acetabular shellClass III
    ++EPRS15040000BUH
  • XLMOB cemented acetabular shellClass III
    ++EPRS15050000BUW
  • XLMOB conventional PE acetabular insertClass III
    ++EPRS16080000BWQ
  • XLMOB crosslinked polyethylene acetabular insertClass III
    ++EPRS16180000BX9

Linked SSCPs

  • SSCP DEV092

Documents

LanguagesENFR