Coils
NumenFR
by MicroPort NeuroTech (Shanghai) Co., Ltd.
A noninvasive, hand-held, electrically-powered unit intended to deliver a low-level electric current to break the connection between a vascular implantable device (typically a neurovascular or peripheral embolization coil or stent) and its deployment device (i.e., implant inserter or delivery wire) via an electrolytic reaction. It is intended to connect to the proximal end of an appropriate implant inserter (delivery wire) which conducts the current to the electrically-unstable detachment point. This is a single-use device.
NumenFR models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| E101 | — | MR Unsafe | Available |
FDA clearances
- 510(k) K260351 May 2026
- 510(k) K242154 September 2024
- 510(k) K232955 January 2024
- 510(k) K203625 September 2021
Procedures that use coils
Frequently asked questions
What is NumenFR used for?
A noninvasive, hand-held, electrically-powered unit intended to deliver a low-level electric current to break the connection between a vascular implantable device (typically a neurovascular or peripheral embolization coil or stent) and its deployment device (i.e., implant inserter or delivery wire) via an electrolytic reaction. It is intended to connect to the proximal end of an appropriate implant inserter (delivery wire) which conducts the current to the electrically-unstable detachment point. This is a single-use device.
Who makes NumenFR?
NumenFR is made by MicroPort NeuroTech (Shanghai) Co., Ltd.. It is listed under embolization coils in our device library.
What sizes does NumenFR come in?
The FDA device database does not list sizes for NumenFR. Check the instructions for use or ask a MicroPort NeuroTech (Shanghai) Co., Ltd. representative.
Is NumenFR MRI safe?
The FDA device database lists NumenFR as MR Unsafe. Always follow the specific MRI conditions in the labeling.
Is NumenFR FDA cleared?
NumenFR is covered by FDA submissions K203625, K232955, K242154, K260351.
How do I contact a MicroPort NeuroTech (Shanghai) Co., Ltd. sales representative?
MicroPort NeuroTech (Shanghai) Co., Ltd. has not listed representatives on LA Vascular yet. Visit the MicroPort NeuroTech (Shanghai) Co., Ltd. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.