Std Med, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Std Med, Inc. makes
Std Med, Inc. manufactures urinary drainage systems, including the STD MED PRIMO PORT and STD MED PRIMO PORT POLY, which are designed for catheterization and bladder management in medical settings.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Std Med Primo Port Ref K070911
Regimes: 510(k) Registry: 510(k)Std Med Primo Port Poly Ref K080645
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Std Med, Inc. have in the registry?
The registry currently lists 2 devices for Std Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Std Med, Inc.'s devices?
Among its 2 most recently registered devices, Std Med, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Std Med, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Std Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Std Med, Inc. in the registry?
The most recently registered devices listed for Std Med, Inc. include STD MED PRIMO PORT and STD MED PRIMO PORT POLY.