Pharma-Plast Intl. A/S
Country not established
- Devices
- 2
What Pharma-Plast Intl. A/S makes
Pharma-Plast Intl. A/S manufactures subcutaneous infusion sets, including the Pureline Basic, Pureline Contact, Pureline Comfort, and ClinI Sofs Plus variants. These devices are designed for continuous infusion of fluids or medications under the skin, supporting long-term therapies such as insulin delivery or chemotherapy.
The company’s infusion sets are regulated under FDA 510(k) clearance, with products classified as Class I and Class II medical devices. The portfolio is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Pharma-Plast Pureline(Tm) Basic(Tm) And Pureline(Tm) Contact(Tm) Subcutaneous Infusion Sets Ref K945617
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pharma-Plast Intl. A/S have in the registry?
The registry currently lists 2 devices for Pharma-Plast Intl. A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pharma-Plast Intl. A/S's devices?
Among its 2 most recently registered devices, Pharma-Plast Intl. A/S has devices listed in FDA 510(k) (2 devices).
What risk classes do Pharma-Plast Intl. A/S's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pharma-Plast Intl. A/S's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pharma-Plast Intl. A/S in the registry?
The most recently registered devices listed for Pharma-Plast Intl. A/S include PHARMA-PLAST PURELINE(TM) BASIC(TM) AND PURELINE(TM) CONTACT(TM) SUBCUTANEOUS INFUSION SETS and PHARMA-PLAST PURELINE(TM) COMFORT(TM) & CLINI SOFS PLUS SUBCUTANEOUS INFUSION SET.