Hedd Roz Canada, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
What Hedd Roz Canada, Inc. makes
Hedd Roz Canada, Inc. manufactures powdered medical examination gloves, including ambidextrous and anatomically correct styles, designed for clinical and procedural use.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Latex Med.exam.gloves Powdered Ambidextrous Ref K915126
Regimes: CE IVDR CE IVDD 510(k) Registry: 510(k)Med.exam.gloves Powdered Anatomically Correct Ref K915127
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hedd Roz Canada, Inc. have in the registry?
The registry currently lists 2 devices for Hedd Roz Canada, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hedd Roz Canada, Inc.'s devices?
Among its 2 most recently registered devices, Hedd Roz Canada, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hedd Roz Canada, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hedd Roz Canada, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hedd Roz Canada, Inc. in the registry?
The most recently registered devices listed for Hedd Roz Canada, Inc. include LATEX MED.EXAM.GLOVES POWDERED AMBIDEXTROUS and MED.EXAM.GLOVES POWDERED ANATOMICALLY CORRECT.