Thermogard HQTM Start-Up Kit EX - The ZOLL® Intravascular Temperature Management - Zoll Circulation, Inc.

Duns Number:799455241

Device Description: The ZOLL® Intravascular Temperature Management (IVTM™) System is comprised of an external The ZOLL® Intravascular Temperature Management (IVTM™) System is comprised of an external heat exchange console (Thermogard HQ™ console) and intravascular heat exchange catheter connected via a sterile heat exchanger and tubing circuit (Thermogard HQTM Start-Up Kit or Thermogard HQTM Start-Up Kit EX). These components together comprise a patient temperature regulation apparatus employing feedback control. The subject devices of this submission are the proposed Thermogard HQTM Console, Thermogard HQTM Start-Up Kit and Thermogard HQTM Start-Up Kit EX.

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More Product Details

Catalog Number

8700-001028-01

Brand Name

Thermogard HQTM Start-Up Kit EX

Version/Model Number

TG2-500D, Extended Length

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Safe

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

NCX

Product Code Name

System, Hypothermia, Intravenous, Cooling

Device Record Status

Public Device Record Key

91f6df7e-82a9-420a-be2a-277f0ff49cb6

Public Version Date

July 05, 2022

Public Version Number

1

DI Record Publish Date

June 27, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ZOLL CIRCULATION, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 331
3 A medical device with high risk that requires premarket approval 1