Queisser Pharma GmbH & Co. KG
Germany DE-MF-000005291 Last updated 17 Sep 2026
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- Devices
- 9
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Protefix Haft-Creme Neutral Ref 04009932002164
Protefix Haft-Creme mit Aloe Vera Ref 04009932002171
Protefix Wund- und Schutzgel Ref 04009932132427
Protefix Haft-Polster Unterkiefer Ref 04009932002218
Protefix Haft-Polster Oberkiefer Ref 04009932002201
Protefix Haft-Creme Minze Ref 04009932522181
Protefix Haft-Pulver Ref 04009932002102
Protefix Haft-Creme Classic Ref 04009932002133
Protefix Haft-Creme Premium Ref 04009932003109
About
Explore the world of Queisser Pharma, with quality products in pharmaceuticals, medical devices, dietary supplements and cosmetics. Here!
What Queisser Pharma GmbH & Co. KG makes
Queisser Pharma produces topical medical adhesives and wound care products, including neutral and flavoured adhesive creams (such as aloe vera and mint), adhesive powders, and adhesive pads designed for the upper and lower jaws. Their portfolio also includes wound and protective gels intended for skin preparation and protection during medical procedures.
All listed devices fall under EU Class I medical devices and are registered in the EU’s eudamed database. The company is based in Germany.
Frequently asked questions
What types of medical devices does Queisser Pharma GmbH & Co. KG manufacture?
Queisser Pharma GmbH & Co. KG specialises in topical medical adhesives and wound care products. Their portfolio includes adhesive creams (such as neutral, aloe vera, and mint-flavoured variants), adhesive powders, and adhesive pads designed for the upper and lower jaws. They also produce wound and protective gels intended for skin preparation and protection during medical procedures.
Where is Queisser Pharma GmbH & Co. KG based?
The company is headquartered in Germany, as indicated by its country designation (DE). This location aligns with its compliance requirements for EU medical device regulations.
Which regulatory registries list Queisser Pharma’s medical devices?
Queisser Pharma’s devices are registered in the eudamed database, which is the official EU portal for medical device information. This registry is used to track devices authorised under EU medical device legislation.
How are Queisser Pharma’s medical devices classified under EU regulations?
All of Queisser Pharma’s listed devices fall under EU Class I, the lowest risk category for medical devices. This classification is determined based on their intended use and risk profile, as defined by EU Medical Device Regulation (MDR) or Medical Device Directive (MDD).
Information
- Country
- Germany
- Address
- 74, Schleswiger Straße, Flensburg, Germany
- Website
- www.queisser.de
- [email protected]
- PRRC contact
- Ebba Loeck
- EUDAMED SRN
- DE-MF-000005291