Medical Disposables Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Medical Disposables Intl., Inc. makes
Medical Disposables Intl., Inc. manufactures single-use medical devices including percutaneous introducer sheath sets, Tyvek-polymer pouches for sterile packaging, arterial line kits, hemodialysis catheters (Hemo-Cath I and II), and needle sets for arteriovenous fistula access.
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
Percutaneous Introducer Sheath Set Ref K771230
Regimes: 510(k) Registry: 510(k)Pouch, Tyvek-Polymylon Ref K770945
Regimes: 510(k) Registry: 510(k)Arteoial Line Kit Ref K771231
Regimes: 510(k) Registry: 510(k)Hemo-Cath I, Kidney Dialysis Catheter Ref K761078
Regimes: 510(k) Registry: 510(k)Catheter, Kidney Dialysis, Hemo-Cath Ii Ref K770552
Regimes: 510(k) Registry: 510(k)Needle Set, A-V Fistula Ref K770699
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Disposables Intl., Inc. have in the registry?
The registry currently lists 6 devices for Medical Disposables Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Disposables Intl., Inc.'s devices?
Among its 6 most recently registered devices, Medical Disposables Intl., Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Medical Disposables Intl., Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Medical Disposables Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Disposables Intl., Inc. in the registry?
The most recently registered devices listed for Medical Disposables Intl., Inc. include PERCUTANEOUS INTRODUCER SHEATH SET, POUCH, TYVEK-POLYMYLON, ARTEOIAL LINE KIT and HEMO-CATH I, KIDNEY DIALYSIS CATHETER.