Barriermed, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Barriermed, Inc. makes
Barriermed, Inc. manufactures powder-free synthetic examination and surgical gloves made from polyisoprene and polychloroprene blends. These include examination gloves for medical procedures and surgical gloves designed for sterile use in operating rooms. The company also produces patient examination gloves tailored for clinical assessments.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via 510(k) clearance. These devices are intended for use in the United States.
Catalogue
Synthalon Pi Powder-Free Synthetic Polyisoprene/Polychloroprene Examination Gloves Mdl 1362-10 To 1362-44 Ref K060733
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Patient Examination Glove Ref K890974
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Barriermed, Inc. have in the registry?
The registry currently lists 3 devices for Barriermed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Barriermed, Inc.'s devices?
Among its 3 most recently registered devices, Barriermed, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Barriermed, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Barriermed, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Barriermed, Inc. in the registry?
The most recently registered devices listed for Barriermed, Inc. include SYNTHALON PI POWDER-FREE SYNTHETIC POLYISOPRENE/POLYCHLOROPRENE EXAMINATION GLOVES MDL 1362-10 TO 1362-44, BARRIERPLUS POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVES and PATIENT EXAMINATION GLOVE.