Verity Medical Ltd.
IE-MF-000007426 · Ireland · Co. Wexford
Verity Medical Ltd. is registered in the European database on medical devices as a manufacturer, with 21 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 21 |
|---|
Most frequent device types declared: NTS500.
Among these devices, 20 are declared active.
Devices declared under this manufacturer
- Kegel8® Mother Nurture
- Kegel8® MultiTone
- Kegel8® Ultra 20
- Kegel8® V for Men
- Kegel8®Ultra
- NeuroTrac PC Software
- NeuroTrac® MultiTENS
- NeuroTrac® MyoPlus2 Pro
- NeuroTrac® Obstetric TENS
- NeuroTrac® Primera
- NeuroTrac® REHAB
- NeuroTrac® SPORTS
Showing 12 of 21 declared devices.
Catalogue references include C6V350, C6V350ZM, ECS310A, ECS401A, NTS500, OPH202.
European nomenclature codes declared: Z12062899, Z12062482.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 21 |
| Country of registration | Ireland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 21 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | VERITY MEDICAL LTD. |
What it holds in Canada
| Licences on record | 4 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 4 |
| First licensed | 2011-01-07 |
Licence types: Device Family (2), Single Device (2).
Licensed under: EMG-BIOFEEDBACK STIMULATORS, NEURO STIMULATORS, REFERENCE(REF) LEADWIRE, WHITE DUAL CONDUCTOR LEADWIRES.
North American profile: Canada only. Verity Medical Ltd. holds a Canadian licence but was not found in the U.S. register.