Loseff Medical Designers, Ltd.
Country not established
- Devices
- 2
What Loseff Medical Designers, Ltd. makes
Loseff Medical Designers, Ltd. manufactures medical devices including a balloon retention chest catheter for drainage applications and a balloon-type self-retention wound catheter for wound management, designed to remain securely in place within the body.
The company’s portfolio includes Class I and Class II devices, with products listed under the FDA’s 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Balloon Retention Chest Catheter Ref K802025
Regimes: 510(k) Registry: 510(k)Loseff Balloon Type Self-Retention Wound Ref K801349
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Loseff Medical Designers, Ltd. have in the registry?
The registry currently lists 2 devices for Loseff Medical Designers, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Loseff Medical Designers, Ltd.'s devices?
Among its 2 most recently registered devices, Loseff Medical Designers, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Loseff Medical Designers, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Loseff Medical Designers, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Loseff Medical Designers, Ltd. in the registry?
The most recently registered devices listed for Loseff Medical Designers, Ltd. include BALLOON RETENTION CHEST CATHETER and LOSEFF BALLOON TYPE SELF-RETENTION WOUND.