MicroPort CRM USA, Inc.
Country not established
- Devices
- 7
Catalogue
- Regimes: PMA Registry: PMA
- Regimes: PMA, withdrawn Registry: PMA
Paradym CRT-D; Paradym RF CRT-D (ZL101), (ZL102); Intensia CRT-D; Platinium CRT-D 1711, 1741. Ref P060027
Regimes: PMA Registry: PMAStelix Ii Endocardial Pacing Leads Ref P020030
Regimes: PMA Registry: PMAOvatio Vr/Dr Ref P980049
Regimes: PMA Registry: PMANon-Rate Responsive Pacemakers Ref P900022
Regimes: PMA Registry: PMASMARTVIEW hotspot Ref P950029
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does MicroPort CRM USA, Inc. have in the registry?
The registry currently lists 7 devices for MicroPort CRM USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MicroPort CRM USA, Inc.'s devices?
Among its 7 most recently registered devices, MicroPort CRM USA, Inc. has devices listed in FDA PMA (7 devices).
What risk classes do MicroPort CRM USA, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for MicroPort CRM USA, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from MicroPort CRM USA, Inc. in the registry?
The most recently registered devices listed for MicroPort CRM USA, Inc. include VEGA Steroid-Eluting Endocardial Leads (VEGA™ R45, VEGA™ R52, and VEGA™ R58), ANGEION SENTINEL IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (ICD)SYSTEM AND THE ANGEFLEX TM DEFIBRILLATION LEAD SYSTEM., Paradym CRT-D; Paradym RF CRT-D (ZL101), (ZL102); Intensia CRT-D; Platinium CRT-D 1711, 1741. and STELIX II ENDOCARDIAL PACING LEADS.