Derlin Company, Ltd.
Country not established
- Devices
- 2
What Derlin Company, Ltd. makes
Derlin Company, Ltd. manufactures powder-free, poly-coated patient examination gloves made from nitrile, designed for medical and clinical use to reduce allergic reactions and improve tactile sensitivity during procedures.
The company’s portfolio is regulated under FDA’s Class I device classification, with products listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Derlin Ref K964817
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Derlin Company, Ltd. have in the registry?
The registry currently lists 2 devices for Derlin Company, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Derlin Company, Ltd.'s devices?
Among its 2 most recently registered devices, Derlin Company, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Derlin Company, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Derlin Company, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Derlin Company, Ltd. in the registry?
The most recently registered devices listed for Derlin Company, Ltd. include DERLIN and NITRILE, POWDER FREE, POLY COATED PATIENT EXAMINATION GLOVES.