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Brk™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical Cardiovascular Division

Identity

Trade Name
BRK™ FDA UDI
Generic Name
Cardiac transseptal needle, single-use FDA UDI
Device Name
Transseptal Needle FDA UDI
Model / Reference
407200 FDA UDI
Description
Transseptal Needle FDA UDI

Identifiers

Catalog Number
407200 FDA UDI
Primary DI / UDI-DI
05414734205092 FDA UDI
FDA Product Code
DRC FDA UDI
GMDN Term
Cardiac transseptal needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1390 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

Yes

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
Outer Diameter — 1.3 Millimeter FDA UDI
Length — 71 Centimeter FDA UDI

Category: Cardiac transseptal needle, single-use

Brk™ by St. Jude Medical Cardiovascular Division — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac transseptal needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5c83aa42-78f9-4ec4-9c20-f7751e9038bd 37 fields · synced May 30, 2026