Catalog Number

CK000482

Brand Name

Per-Q-Cath

Version/Model Number

CK000482

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

-

Product Code

LJS

Product Code Name

Catheter,intravascular,therapeutic,long-term greater than 30 days

Public Device Record Key

5d737b88-d303-44d2-9890-fe79910320c2

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

September 24, 2015

Package DI Number

10801741104340

Quantity per Package

2

Contains DI Package

00801741104343

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA