Ferti-lily Conception Aid Cup

Primary DI

01220000223905

Basic UDI-DI Code

122000022PROJ60KP

Reference

Ferti-lily Conception Aid Cup

Device Types

None provided

Regulation

Eu Mdr

Classification

Eu Md Class 1

Status

On The Market

Manufacturer

Fridababy, LLC

Use according to the directions provided. • You may experience light cramping during the first use. • Do not pull on the stem of the cup with force. The stem can break with excessive force and while it can be used to remove the cup slowly, one should not pull on the ball of the stem with force, but use the stem to remove the cup little by little. • The FERTI-LILY Cup is not a contraceptive device and will not protect you against sexually transmitted infections. • The FERTI-LILY Cup and TSS: There is no known link between Toxic Shock Syndrome (TSS) and cups such as the FERTI-LILY Cup. Consult your physician prior to using the FERTI-LILY Cup if you have previously been diagnosed with TSS. TSS is a rare condition, usuall associated with the use of tampons, whose symptoms must be taken seriously. Remove the FERTI-LILY Cup and contact your doctor immediately if you experience any of the following symptoms: sudden vomiting, diarrhea, high fever, headache, a sunburn-like rash, muscle aches, confusion or seizures. • Do not use the FERTI-LILY Cup if you have a yeast or bacterial infection. Resume use once the infection has completely cleared. If you have used the FERTI-LILY Cup while you have had an infection, it is recommended that you replace your cup with a new one to ensure against repeat infection. • Dispose in trash. Do not f lush the FERTI-LILY Cup down the toilet. • If you experience any adverse effects, discontinue use and consult with your doctor. FERTI-LILY helps to increase the amount of sperm that swims into the cervix. There are many factors that could influence fertility on which FERTI-LILY cannot have any influence. If you are still not pregnant after 12 months of tr ying or are worried about your fertility, please consult with your doctor. This device is intended as an aid in conception and does not guarantee pregnancy. Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the local competent authority.

The Basic UDI-DI associated with this device has 6 devices in total. Below are some other devices sharing the same Basic UDI-DI.

Other on-the-market devices with the same classification (Eu Md Class 1) and regulation (EU MDR).