truFreeze - truFreeze Aire PV Passive Venting Catheter Kit - US Endoscopy

Duns Number:627879687

Device Description: truFreeze Aire PV Passive Venting Catheter Kit includes 7 Fr Catheter, Straight Spray Cat truFreeze Aire PV Passive Venting Catheter Kit includes 7 Fr Catheter, Straight Spray Catheter Introducer and is used with the truFreeze Spray Cryotherapy System.

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More Product Details

Catalog Number

CO8407030501

Brand Name

truFreeze

Version/Model Number

CO8407030501

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

bd45ee56-d833-4abe-84f0-bd60bc68da59

Public Version Date

October 04, 2022

Public Version Number

2

DI Record Publish Date

May 04, 2022

Additional Identifiers

Package DI Number

10724995199286

Quantity per Package

5

Contains DI Package

00724995199289

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