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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 39411

Rev. 1Issued
Valid until
Sep 20, 2028

Overview

Certificate number
39411
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0459394111

Validity

Issued
Apr 7, 2025
Valid from
Apr 7, 2025
Valid until
Sep 20, 2028

Manufacturer

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

Notified body

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

Covered devices

  • ceramic femoral headClass III
    ++EPRS13030000BSW

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

Unspecified1

1 scope

  • ceramic femoral head
    ++EPRS13030000BSW

Documents

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