CINOGY GmbH
Germany DE-MF-000048574 Last updated 8 Jun 2026
- Devices
- 14
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Spacer PlasmaDerm Cutan Ref 22101
Spacer PlasmaDerm Flex Ref 22200
Spacer PlasmaDerm Flex (SU 12 pcs.) Ref 22212
Spacer PlasmaDerm Cutan (SU 10 pcs.) Ref 22110
Spacer PlasmaDerm Flex (SU 24 pcs.) Ref 22224
Spacer Dress Wound Care Ref 24000
PlasmaDerm Vario, Model PlasmaDerm Flex Ref K25200
PlasmaDerm Dress Ref K25400
Spacer PlasmaDerm Cutan (SU 80 pcs.) Ref 22180
PlasmaDerm Vario, Model PlasmaDerm Flex (CH) Ref K25204
EUDAMED certificates
Eurofins Electric & Electronics Finland Oy 0537 1 certificate
- CR-03-1211-881-25 Issued
Quality management system EU MDR
- Issued
- 14 Aug 2025
- Expires
- 14 Aug 2030
Related companies
Notified bodies
What CINOGY GmbH makes
CINOGY GmbH makes PlasmaDerm spacer and wound care devices, including the PlasmaDerm Flex and PlasmaDerm Cutan models, which are designed for topical plasma therapy applications. These products are supplied in various sterile unit pack sizes, such as SU 8, SU 10, SU 12, SU 24, and SU 80 pieces, and include wound dressings and universal variomodels for clinical use.
The manufacturer's devices are classified as Class IIa and Class IIb under the EU regulatory framework and are listed in the EUDAMED database. CINOGY GmbH is based in Germany.
Frequently asked questions
What does CINOGY GmbH make?
CINOGY GmbH makes PlasmaDerm spacer and wound care devices, including the PlasmaDerm Flex and PlasmaDerm Cutan models, which are designed for topical plasma therapy applications. These products are supplied in various sterile unit pack sizes, such as SU 8, SU 10, SU 12, SU 24, and SU 80 pieces, and include wound dressings and universal variomodels for clinical use.
Where is CINOGY GmbH based?
CINOGY GmbH is based in Germany, as stated in the manufacturer's summary and country code DE, which indicates its location within the European Union.
Which registries list CINOGY GmbH's devices?
CINOGY GmbH's devices are listed in the EUDAMED database, which is the European Union's medical device registry used for tracking devices placed on the market under the EU regulatory framework.
How are CINOGY GmbH's devices classified?
CINOGY GmbH's devices are classified as Class IIa and Class IIb under the EU regulatory framework, indicating they are medium-risk devices requiring conformity assessment by a notified body for market placement.
Information
- Country
- Germany
- Address
- 7, Charlottenburger Straße, Duderstadt, Germany
- Website
- www.plasmaderm.de
- [email protected]
- Phone
- +495527746970
- PRRC contact
- Matthias Kopp
- EUDAMED SRN
- DE-MF-000048574