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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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EPflex Feinwerktechnik GmbH

Certificate 1000266008

Rev. 01Issued
Valid until
Jul 2, 2029

Certificate 1000266008 is a valid Technical documentation issued to EPflex Feinwerktechnik GmbH and registered in EUDAMED. Valid until July 2, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
1000266008
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0297100026600801

Validity

Issued
Oct 27, 2025
Valid from
Oct 27, 2025
Valid until
Jul 2, 2029

Notified body

Notified body
DQS Medizinprodukte GmbH
Notified body SRN
0297
Notified body country
Germany

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

  • Guidewires for Central Circulatory Application
    42556056gwcIIIEH

Manufacturer

Manufacturer
EPflex Feinwerktechnik GmbH
Manufacturer SRN
DE-MF-000005425
Manufacturer country
Germany

Covered devices

  • Guidewires for Central Circulatory ApplicationClass III
    42556056gwcIIIEH

Linked SSCPs

  • SSCP SSCP_gwlll

Documents

LanguagesDEEN