respistim R Stimulation Lead, Inline Connector 3652
by Respicardia United States GUDID
Product code PSR
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00857688007452 | Date20 Aug 2021 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- respistim R Stimulation Lead, Inline Connector
- Generic Name
- Transvenous phrenic nerve electrical stimulation control unit
- Model / Reference
- 3652
- Primary DI / UDI-DI
- 00857688007452
- PMA Number
- FDA Product Code
- PSR
- GMDN Term
- Transvenous phrenic nerve electrical stimulation control unit
- Device Class
- Class III
- Commercial Distribution
- In Commercial Distribution
- MRI Safety
- MR Unsafe
Other devices from Respicardia
Properties & raw data
Show properties, registry sources and raw records
Other properties (7)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
Sources (1)
- FDA UDI d741fc1f-f14f-4330-af54-56106f9ec547