P/L Biomedical
Country not established
- Devices
- 3
What P/L Biomedical makes
P/L Biomedical makes pen needles and subcutaneous infusion sets, including the ClickFine Pen Needle and the Maersk Medical PureLine Comfort Subcutaneous Infusion Set.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Clickfine Pen Needle Ref K122971
510(k) 510(k)Clickfine Pen Needle Ref K122969
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does P/L Biomedical have in the registry?
The registry currently lists 3 devices for P/L Biomedical. Devices recorded under merged duplicate company entries are counted once.
Which registries list P/L Biomedical's devices?
Among its 3 most recently registered devices, P/L Biomedical has devices listed in FDA 510(k) (3 devices).
What risk classes do P/L Biomedical's devices fall under?
Among its 3 most recently registered devices, the classes recorded for P/L Biomedical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from P/L Biomedical in the registry?
The most recently registered devices listed for P/L Biomedical include CLICKFINE PEN NEEDLE and MAERSK MEDICAL PURELINE COMFORT SUBCUTANEOUS INFUSION SET.