Pharma-Plast, Ltd.
United KingdomFDA applicant, unverified
Part of Pharmaplast
- Devices
- 1
What Pharma-Plast, Ltd. makes
Pharma-Plast, Ltd. manufactures the STERISEAL OPHTHALMIC CANNULA, a sterile medical device used in ophthalmic procedures for fluid drainage or infusion.
The STERISEAL OPHTHALMIC CANNULA is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Steriseal Ophthalmic Cannula Ref K943932
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pharma-Plast, Ltd. have in the registry?
The registry currently lists 1 device for Pharma-Plast, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pharma-Plast, Ltd.'s devices?
Among its 1 most recently registered device, Pharma-Plast, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Pharma-Plast, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pharma-Plast, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pharma-Plast, Ltd. in the registry?
The most recently registered devices listed for Pharma-Plast, Ltd. include STERISEAL OPHTHALMIC CANNULA.