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FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH

Germany DE-MF-000005284 Last updated 21 Oct 2026

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Devices
202
Registries
EUDAMED
FDA recalls
0

Catalogue202

Page 1 of 5

  • IP071015F1 Ref IP071015F1

    Class III EUDAMED Active

  • PV610813F3 Ref PV610813F3

    Class IIb EUDAMED Active

  • PV101015F3 Ref PV101015F3

    Class IIb EUDAMED Active

  • IP070417F1 Ref IP070417F1

    Class IIb EUDAMED Active

  • PV610712F1 Ref PV610712F1

    Class IIb EUDAMED Active

  • PV162030F2 Ref PV162030F2

    Class IIb EUDAMED Active

  • PV110715F5 Ref PV110715F5

    Class IIb EUDAMED Active

  • PV091530F1 Ref PV091530F1

    Class IIb EUDAMED Active

  • PV121015F1 Ref PV121015F1

    Class IIb EUDAMED Active

  • PV750424F10 Ref PV750424F10

    Class IIb EUDAMED Active

  • PV141015F10 Ref PV141015F10

    Class IIb EUDAMED Active

  • IP072415F1 Ref IP072415F1

    Class IIb EUDAMED Active

  • PV121015F3 Ref PV121015F3

    Class IIb EUDAMED Active

  • PV161010F3 Ref PV161010F3

    Class IIb EUDAMED Active

  • PV101015F1 Ref PV101015F1

    Class IIb EUDAMED Active

  • PV101317F3 Ref PV101317F3

    Class IIb EUDAMED Active

  • IP073045F1 Ref IP073045F1

    Class IIb EUDAMED Active

  • IP081520F1 Ref IP081520F1

    Class IIb EUDAMED Active

  • PV092030F2 Ref PV092030F2

    Class IIb EUDAMED Active

  • IP071520F1 Ref IP071520F1

    Class IIb EUDAMED Active

  • PV131217F1 Ref PV131217F1

    Class IIb EUDAMED Active

  • PV540315F3 Ref PV540315F3

    Class IIb EUDAMED Active

  • PV360423F1 Ref PV360423F1

    Class IIb EUDAMED Active

  • PV164560F1 Ref PV164560F1

    Class IIb EUDAMED Active

  • PV161525F2 Ref PV161525F2

    Class IIb EUDAMED Active

  • PV100715F3 Ref PV100715F3

    Class IIb EUDAMED Active

  • PV100715F1 Ref PV100715F1

    Class IIb EUDAMED Active

  • PV130914F3 Ref PV130914F3

    Class IIb EUDAMED Active

  • PV101015F10 Ref PV101015F10

    Class IIb EUDAMED Active

  • PV091010F5 Ref PV091010F5

    Class IIb EUDAMED Active

  • PV131217F5 Ref PV131217F5

    Class IIb EUDAMED Active

  • PV500423F3 Ref PV500423F3

    Class IIb EUDAMED Active

  • PV780318F1 Ref PV780318F1

    Class IIb EUDAMED Active

  • PV160735F1 Ref PV160735F1

    Class IIb EUDAMED Active

  • PV094020F1 Ref PV094020F1

    Class IIb EUDAMED Active

  • PV091525F1 Ref PV091525F1

    Class IIb EUDAMED Active

  • PV781715F1 Ref PV781715F1

    Class IIb EUDAMED Active

  • IP103316F1 Ref IP103316F1

    Class IIb EUDAMED Active

  • PV162030F5 Ref PV162030F5

    Class IIb EUDAMED Active

  • PV160010F3 Ref PV160010F3

    Class IIb EUDAMED Active

  • IP071515F3 Ref IP071515F3

    Class IIb EUDAMED Active

  • PV110715F3 Ref PV110715F3

    Class IIb EUDAMED Active

  • PV740203F1 Ref PV740203F1

    Class IIb EUDAMED Active

  • PV350323F1 Ref PV350323F1

    Class IIb EUDAMED Active

  • PV740404F3 Ref PV740404F3

    Class IIb EUDAMED Active

  • IP080706F5 Ref IP080706F5

    Class IIb EUDAMED Active

  • PV111015F3 Ref PV111015F3

    Class IIb EUDAMED Active

  • IVT01F1 Ref IVT01F1

    Class I EUDAMED Active

  • IP082432F1 Ref IP082432F1

    Class IIb EUDAMED Active

  • PV141515F1 Ref PV141515F1

    Class IIb EUDAMED Active

Showing 1-50 of 202

EUDAMED certificates5

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (5)

TÜV SÜD Product Service GmbH 0123 5 certificates

  • G70 107055 0007 Issued

    Technical documentation EU MDR

    Issued
    13 Mar 2024
    Expires
    12 Mar 2029
  • G70 107055 0006 Issued

    Technical documentation EU MDR

    Issued
    26 Feb 2024
    Expires
    25 Feb 2029
  • G70 107055 0005 Issued

    Technical documentation EU MDR

    Issued
    26 Sep 2023
    Expires
    25 Sep 2028
  • G15 107055 0012 Issued

    Quality management system EU MDR

    Issued
    5 Feb 2026
    Expires
    5 Sep 2027
  • G70 107055 0003 Issued

    Technical documentation EU MDR

    Issued
    10 Aug 2022
    Expires
    9 Aug 2027

Related companies

Notified bodies

About

The FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH (FEG) was founded in 1992 in Aachen und has since been known for extraordinary innovations in textile technology. With highly motivated und well-trained employees, proprietary Forschungs and development capacities und intelligent production plants, the FEG Textiltechnik is today Germany's leading manufacturer of medical textile implants. Under the globally protected brand name DynaMesh®, [...]

Translated from the manufacturer's own website. Source

What FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH makes

FEG Textiltechnik develops and manufactures medical textile implants, including products such as the DynaMesh® line, which are designed for surgical applications. Their portfolio includes devices like PV610813F3, PV101015F3, and IP070417F1, which are likely intended for hernia repair, soft tissue reinforcement, or similar reconstructive procedures. These products are engineered using textile-based materials to provide structural support in surgical contexts.

The company’s devices fall under EU medical device classifications, including Class I and Class IIb, and are registered in the eudamed database. Their products are listed for use within the European Union’s regulatory framework, adhering to applicable conformity assessment procedures for their respective risk categories. The manufacturer operates from Germany.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH manufacture?

FEG Textiltechnik specializes in developing and manufacturing medical textile implants. These devices are designed for surgical applications, such as hernia repair or soft tissue reinforcement, and are constructed using textile-based materials to provide structural support. Examples of their products include devices like PV610813F3 and PV101015F3, which are likely intended for reconstructive procedures.

Where is FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH based?

FEG Textiltechnik is headquartered in Germany, specifically in Aachen. The company operates from this location, focusing on research, development, and production of its medical textile implants.

Which regulatory registries list FEG Textiltechnik’s medical devices?

FEG Textiltechnik’s medical devices are registered in the eudamed database, which is the official EU registry for medical devices. This listing ensures transparency and compliance with the European Union’s regulatory requirements for medical devices.

How are FEG Textiltechnik’s medical devices classified under EU regulations?

FEG Textiltechnik’s devices are classified under the EU Medical Device Regulations (MDR) as either Class I or Class IIb. The classification depends on the intended use and risk associated with each product—Class IIb applies to higher-risk devices like those used in reconstructive surgeries, while Class I covers lower-risk items. These classifications determine the conformity assessment procedures required before market placement.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Germany
Address
70, Prager Ring, Aachen, Germany
Phone
+49 241 1892374-0
PRRC contact
Claudia Barz
EUDAMED SRN
DE-MF-000005284