Jextrag Schaffhausen AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Jextrag Schaffhausen AG makes
Jextrag Schaffhausen AG manufactures latex patient examination gloves, designed for clinical use in medical examinations and procedures.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891880
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jextrag Schaffhausen AG have in the registry?
The registry currently lists 1 device for Jextrag Schaffhausen AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jextrag Schaffhausen AG's devices?
Among its 1 most recently registered device, Jextrag Schaffhausen AG has devices listed in FDA 510(k) (1 device).
What risk classes do Jextrag Schaffhausen AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jextrag Schaffhausen AG's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jextrag Schaffhausen AG in the registry?
The most recently registered devices listed for Jextrag Schaffhausen AG include PATIENT EXAMINATION GLOVES (LATEX).