Granton Medical, Ltd.
Country not established
- Devices
- 2
What Granton Medical, Ltd. makes
Granton Medical, Ltd. manufactures self-seal sterilization pouches designed for medical device sterilization processes, including those using steam or ethylene oxide. These pouches are intended to provide a barrier that maintains sterility and integrity during storage and transport of sterilized items.
The company’s sterilization pouches are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These products are intended for use in the United States, where they are subject to compliance with the FDA’s medical device reporting requirements.
Catalogue
Self Seal Sterilization Pouch Ref K023025
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Granton Medical, Ltd. have in the registry?
The registry currently lists 2 devices for Granton Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Granton Medical, Ltd.'s devices?
Among its 2 most recently registered devices, Granton Medical, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Granton Medical, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Granton Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Granton Medical, Ltd. in the registry?
The most recently registered devices listed for Granton Medical, Ltd. include SELF SEAL STERILIZATION POUCH and GRANTON MEDICAL 121-135 C SELF-SEAL STERILIZATION POUCHES.