Ferti·lily Conception Gel
Basic Information
- Primary DI
- 01220000223967
- Basic UDI-DI Code
- 122000022PROJ126MN
- Reference
- Ferti·lily Conception Gel
- Device Types
- None provided
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 1
- Status
- On The Market
- Manufacturer
- Fridababy, LLC
Additional Description
For first-time users, if you have sensitive skin you may want to try applying a little gel on the inside of your elbow to test if you are sensitive to its ingredients. Use according to the directions provided. Do not use the product after the expiration date. Check expiry date before use. The FERTl·LILY Conception Gel can be used for 6 months after opening. The FERTl·LILY Conception Gel is not a contraceptive and will not protect you against sexually transmitted infections. Do not use the FERTl•LILY Conception Gel if you have a yeast or bacterial infection or if you have recently had irritations or wounds on the vaginal area. Resume use once the infection has completely cleared. If you experience any adverse effects, discontinue use and consult your physician. Keep out of the reach of children. FERTl·LILY Conception Gel helps to increase the comfort and pleasure of intercourse, without negative impact on sperm motility and survival. There are many factors that could influence fertility on which this product cannot have any effect. If you are still not pregnant after 12 months of trying or are worried about your fertility, please consult your doctor. The FERTl·LILY Conception Gel is intended as an aid to be used while trying to conceive and does not guarantee pregnancy
CND Nomenclature Codes
| Code | Description |
|---|---|
| U0803 | VAGINAL DEVICES IN THE FORM OF SOLUTIONS/CREAMS/OVA/TABLETS |
Available In Countries
Related Devices
The Basic UDI-DI associated with this device has 6 devices in total. Below are some other devices sharing the same Basic UDI-DI.
Ferti·lily Conception Gel
DeviceFerti·lily Conception Gel
DeviceFerti·lily Conception Gel
DeviceFerti·lily Conception Gel
DeviceFerti·lily Conception Gel
DeviceSimilar Devices
Other on-the-market devices with the same classification (Eu Md Class 1) and regulation (EU MDR).