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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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Keri Medical SA

Certificate 28620157857-03

Rev. 03Issued
Valid until
Feb 15, 2028

Overview

Certificate number
28620157857-03
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
286228620157857-0303

Validity

Issued
Mar 20, 2026
Valid from
Mar 20, 2026
Valid until
Feb 15, 2028

Manufacturer

Manufacturer
Keri Medical SA
Manufacturer SRN
CH-MF-000021960
Manufacturer country
Switzerland

Notified body

Notified body
Intertek Medical Notified Body AB
Notified body SRN
2862
Notified body country
Sweden

Covered devices

  • TOUCH CMC1 ProsthesisClass III
    764018116010AV

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
Yes
MOS outside EUDAMED
—
QMS/MOS type
Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

  • TOUCH CMC1 Prosthesis
    764018116010AV

Documents

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