FDA REGISTRATION

Nenesupply products are categorized as Class II medical device by US FDA. The manufacturing facility Nenesupply Co., Ltd. is registered with US FDA. All Nenesupply products are manufactured according to FDA quality control regulations.

EU BPA FREE

All Nenesupply products are tested against EU regulation for BPA. All parts are made from BPA free materials.

 

 

 

 

 

US FDA FOOD CONTACT MATERIAL

All Nenesupply products that “contact milk” are tested against US FDA regulations for food contact plastics material, meaning that “Nenesupply products are FDA compliant for food contacts”. Milk-contact parts include breastshield, valve, duckbill valves, membranes, and bottles. Tubing and backflow protectors do not contact food, so they are only tested against EU BPA.

CA-65 DEHP free

Nenesupply’s pump in style tubing is also tested against California-65. The tubing material is PVC and the test result is DEHP free while most PVC in this industry contains DEHP. Nonetheless, Nenesupply still adopts high quality PVC, and it does NOT contain DEHP.