Schreiner Medipharm
Country not established
- Devices
- 1
What Schreiner Medipharm makes
Schreiner Medipharm manufactures needle-trap and needle safety labels designed to reduce sharps injuries in healthcare settings. These products are intended to secure needles and syringes after use, minimizing the risk of accidental punctures during disposal or handling.
The company’s portfolio is regulated under FDA Class II devices and includes products listed via the 510(k) pathway. These devices are primarily marketed in the United States, where compliance with FDA regulations is required.
Catalogue
Needle-Trap/Needle Safety Label Ref K073206
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schreiner Medipharm have in the registry?
The registry currently lists 1 device for Schreiner Medipharm. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schreiner Medipharm's devices?
Among its 1 most recently registered device, Schreiner Medipharm has devices listed in FDA 510(k) (1 device).
What risk classes do Schreiner Medipharm's devices fall under?
Among its 1 most recently registered device, the classes recorded for Schreiner Medipharm's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schreiner Medipharm in the registry?
The most recently registered devices listed for Schreiner Medipharm include NEEDLE-TRAP/NEEDLE SAFETY LABEL.