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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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Euro Vital Pharma GmbH

Certificate 3827GB448250203

Issued
Valid until
Oct 16, 2027

Overview

Certificate number
3827GB448250203
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
04823827GB448250203

Validity

Issued
Feb 3, 2025
Valid from
Feb 3, 2025
Valid until
Oct 16, 2027

Manufacturer

Manufacturer
Euro Vital Pharma GmbH
Manufacturer SRN
DE-MF-000025194
Manufacturer country
Germany

Notified body

Notified body
DNV MEDCERT GmbH
Notified body SRN
0482
Notified body country
Germany

Covered devices

No specific devices are listed for this certificate.

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
Yes
Intended medical purpose
No
SPP applicable
No
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Class IIb only

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIb1

1 scope

  • MDN 1213 EMDN G0401
    Class IIb

Documents

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