Yes, the Keller Funnel®2 can assist in the delivery of breast, calf, gluteal and pectoral implants, whether they are smooth round, textured round, shaped or anatomical. Textured or anatomical/shaped implants may require the Funnel to be trimmed slightly larger. You will find additional information in our product review video.
The Keller Funnel®2 is intended for single patient use only. It is not to be resterilized or reused. Re-use or resterilization should not be performed under any conditions as contamination or infection may occur. Attempts to re-use or resterilize may cause diminished product performance, including loss of lubricity, potentially causing implant damage, including rupture.
Please access our product review to learn the specifics about using the Keller Funnel®2.
Check out our Doctor Locator to see the list of surgeons using the Funnel in your area. If you don’t see a surgeon in your area, a Keller Medical representative will gladly assist you with your request. Please click to contact our Customer Service department or call us at 772-219-9993.
Open the sterile, double-pouched packaging of the Keller Funnel®2 and submerge the device in sterile solution. We recommend surgeons keep implants in their original packaging, submerged in sterile solution. While the surgeon holds open the wide end of the Keller Funnel®2, the nurse can pour the implant from its original packaging directly into the Funnel. Once tested and loaded properly, the surgeon places the Funnel tip into the prepared pocket and propels the implant into place.
Keller Medical, Inc. has created Instructions For Use available in PDFs in many languages, to ensure information on proper usage is available for the Keller Funnel®2.
Please visit the Collateral Center to view and download the IFU.
Keller Medical, Inc. has compiled information to help facilitate discussions that hospital product board review committees may conduct. You can find it here.
The Keller Funnel®2 has passed multiple biocompatibility tests, both in vivo and in vitro, thus establishing the biocompatibility of the device.
Keller Medical underwrites periodic third-party surveys to obtain surgeons’ experiences using the Funnel.