← Back to catalogue

Fast-Cath™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Fast-Cath™ FDA UDI
Generic Name
Cardiac transseptal access set FDA UDI
Device Name
Transseptal Guiding Introducer FDA UDI
Model / Reference
406851 FDA UDI
Description
Transseptal Guiding Introducer FDA UDI

Identifiers

Catalog Number
406851 FDA UDI
Primary DI / UDI-DI
05414734203401 FDA UDI
510(k) Number
K964518 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Cardiac transseptal access set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 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 — 8.5 French FDA UDI
Length — 63.0000 Centimeter FDA UDI

Category: Cardiac transseptal access set

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

Similar devices

Also classified as Cardiac transseptal access set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e6b4599e-3343-494f-b6f1-ac0fa3a3deeb 38 fields · synced May 30, 2026