Propaq Md 320-2421322-01
Listed
Valid until
Not applicable
FDA recalls
None ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00847946020170 | Date6 Sep 2017 | StatusListed |
Recalls
-
- Terminated Z-1311-2014
Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Propaq Md
- Generic Name
- Rechargeable professional automated external defibrillator
- Model / Reference
- 320-2421322-01
- Description
- Defibrillator ,MAIN ASSY, PROPAQ MONITOR/DEFIBRILLATOR 12 LEAD/W INTERP, PACING, NIBP, SPO2, IBP, TEMP CPR EXPANSION PACK AND ETCO2, W/CP2, DMST
- Primary DI / UDI-DI
- 00847946020170
- FDA Product Code
- MKJ
- GMDN Term
- Rechargeable professional automated external defibrillator
- Device Class
- Class III
- Regulation Number
- 870.5310
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Unsafe
Other devices from Zoll Medical Corporation
Properties
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No