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Livewire™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Livewire™ FDA UDI
Generic Name
Cardiac mapping catheter, percutaneous, single-use FDA UDI
Device Name
Steerable Electrophysiology Catheter FDA UDI
Model / Reference
401905 FDA UDI
Description
Steerable Electrophysiology Catheter FDA UDI

Identifiers

Catalog Number
401905 FDA UDI
Primary DI / UDI-DI
05414734202541 FDA UDI
FDA Product Code
DRF FDA UDI
DRA FDA UDI
GMDN Term
Cardiac mapping catheter, percutaneous, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1220 FDA UDI
870.1280 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 7 French FDA UDI

Category: Cardiac mapping catheter, percutaneous, single-use

Livewire™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac mapping catheter, percutaneous, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
St. Jude Medical, Inc.

Sources (1)

  • FDA UDI 5705df42-f8d1-49d8-9f36-de4662ae956d 37 fields · synced May 31, 2026