Teleflex Medical
IE-MF-000015868 · Ireland · Athlone
Teleflex Medical is registered in the European database on medical devices as a manufacturer, with 1 176 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 619 |
|---|---|
| Class IIa | 557 |
Most frequent device types declared: 121300-000070, 121303-000040, 121903-000100, 858603-000080, IPN041959.
Among these devices, 1 134 are declared sterile, 387 implantable, 1 active, 1 with a measuring function.
Devices declared under this manufacturer
- EZ-IO 25mm Needle + Stabilizer Kit
- Integral ureter stent set
- Integral ureter stent set, central / open
- Liquick X-treme, Intermittent catheter, Tiemann tip, CH14
- Rusch Care CrystalClear Plus, C Tracheostomy Tube Set
- Rusch Care Tracheofix Cough Cap PVC, for Tracheofix Tracheostomy Tube
- Rusch Care Tracheofix TFP, Set PVC, Tracheostomy tube set, phonation
- Rusch CrystalClear Plus Tracheostomy Tube Set
- Rusch CrystalClear Plus, C Tracheostomy Tube Set
- Rusch PercuQuick PVC for use with PDT only, first step Dilator for PDT
- Rusch Tracheofix TF, Set PVC
- TRACFLEX PLUS S TRACHEOSTOMY TUBE SET
Showing 12 of 1 176 declared devices.
Catalogue references include 121903-000100, 123101-000080, 334207-000040, 334714-000070, 858163-000060, 859003-000085.
European nomenclature codes declared: U020302, U010199, A019011, R01020101, R0105020201, R0105010101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | TELEFLEX MEDICAL (IE) · FDA 9616683 |
| Devices in EUDAMED | 1 176 |
| Country of registration | Ireland |
Device-level evidence
| Devices with a numeric GTIN | 1 176 |
|---|---|
| Found in the U.S. device database | 89 |
| Share | 7.6 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | TELEFLEX MEDICAL |
North American profile: Both markets. Teleflex Medical is registered in both the United States and Canada.