truFreeze - Rapid AV Catheter Kit with 20 FR CDT includes - US Endoscopy

Duns Number:627879687

Device Description: Rapid AV Catheter Kit with 20 FR CDT includes 2.1mm Catheter (Straight Spray), Catheter In Rapid AV Catheter Kit with 20 FR CDT includes 2.1mm Catheter (Straight Spray), Catheter Introducer, 20 Fr CryoDecompression Tube (CDT), Dual Lumen, Connector, Suction Tubing and is used with the truFreeze Spray Cryotherapy System.

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More Product Details

Catalog Number

2000177

Brand Name

truFreeze

Version/Model Number

2000177

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K113021,K133258,K143625,K150920,K152668,K160273,K161557,K162695,K163244,K171522,K171626,K172041,K222272,K113021,K133258,K143625,K150920,K152668,K160273,K161557,K162695,K163244,K171522,K171626,K172041,K222272,K113021,K133258,K143625,K150920,K152668,K160273,K161557,K162695,K163244,K171522,K171626,K172041,K222272

Product Code Details

Product Code

GEH

Product Code Name

UNIT, CRYOSURGICAL, ACCESSORIES

Device Record Status

Public Device Record Key

33056b6a-be0f-401d-9486-7a626c5a6b75

Public Version Date

October 04, 2022

Public Version Number

2

DI Record Publish Date

May 04, 2022

Additional Identifiers

Package DI Number

10724995199224

Quantity per Package

5

Contains DI Package

00724995199227

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case

"US ENDOSCOPY" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 51
2 A medical device with a moderate to high risk that requires special controls. 902