Surgiplast, Ltd.
IndiaFDA applicant, unverified
- Devices
- 2
What Surgiplast, Ltd. makes
Surgiplast, Ltd. manufactures disposable syringes and infusion sets, which are single-use medical devices for fluid administration and injection.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Disposable Syringe Ref K950969
Regimes: 510(k) Registry: 510(k)Infusion Set Ref K950970
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgiplast, Ltd. have in the registry?
The registry currently lists 2 devices for Surgiplast, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgiplast, Ltd.'s devices?
Among its 2 most recently registered devices, Surgiplast, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Surgiplast, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Surgiplast, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgiplast, Ltd. in the registry?
The most recently registered devices listed for Surgiplast, Ltd. include DISPOSABLE SYRINGE and INFUSION SET.