Identity
- Trade Name
- PulseSelect™ FDA UDI
- Generic Name
- Cardiac irreversible electroporation system remote control FDA UDI
- Device Name
- REMOTE CONTROL PSRC100 PFA 10 FT US FDA UDI
- Model / Reference
- PSRC100 FDA UDI
- Description
- REMOTE CONTROL PSRC100 PFA 10 FT US FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000617745 FDA UDI
- PMA Number
- P230017 FDA UDI
- FDA Product Code
- QZI FDA UDI
- GMDN Term
- Cardiac irreversible electroporation system remote control FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 10.0 Feet FDA UDI
Category: Cardiac irreversible electroporation system remote control
PulseSelect™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
P230017 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI 6bab06bc-803b-4d6f-a2db-cf2e88a42d59 37 fields · synced May 30, 2026