Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger
Country not established
- Devices
- 1
What Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger makes
Hemo-Sanitas, Inc. manufactures pre-filled syringes designed for single-use medical injections, including those for intravenous, subcutaneous, or intramuscular administration. These syringes are engineered for precision dosing and compatibility with a range of pharmaceutical formulations, including liquids and suspensions. The product line includes both standard and specialized syringe sizes to accommodate different clinical applications.
The company’s syringe portfolio is classified under Class II devices in the US regulatory framework, requiring premarket notification (510(k)) clearance through the FDA. These devices are listed under the 510(k) registry and comply with applicable US medical device regulations. Hemo-Sanitas, Inc. operates from the United States.
Catalogue
Hemo-Sanitas Syringe Ref K884921
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger have in the registry?
The registry currently lists 1 device for Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger's devices?
Among its 1 most recently registered device, Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger has devices listed in FDA 510(k) (1 device).
What risk classes do Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger in the registry?
The most recently registered devices listed for Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger include HEMO-SANITAS SYRINGE.