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PulseSelect™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
PulseSelect™ FDA UDI
Generic Name
Cardiac irreversible electroporation system catheter FDA UDI
Device Name
CATHETER PSCC100 PULSESELECT US 25MM FDA UDI
Model / Reference
PSCC100 FDA UDI
Description
CATHETER PSCC100 PULSESELECT US 25MM FDA UDI

Identifiers

Primary DI / UDI-DI
00763000617554 FDA UDI
PMA Number
P230017 FDA UDI
FDA Product Code
QZI FDA UDI
GMDN Term
Cardiac irreversible electroporation system catheter FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Catheter Working Length — 99.0 Centimeter FDA UDI
Catheter Length — 145.0 Centimeter FDA UDI

Category: Cardiac irreversible electroporation system catheter

PulseSelect™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac irreversible electroporation system catheter.

Cleared under the same submission

P230017 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 4dff35c2-4fb0-4b5d-bc29-f35a6dfcaf55 37 fields · synced Jun 1, 2026