Catalog Number

SC1606

Brand Name

TruCath

Version/Model Number

SC1606

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

-

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

-

FDA Premarket Submission

K142767,K142767,K142767

Product Code

GBM

Product Code Name

CATHETER, URETHRAL

Public Device Record Key

46caa5a7-9f7d-4b63-bd18-85a1f0e2a486

Public Version Date

February 28, 2020

Public Version Number

1

DI Record Publish Date

February 20, 2020

Package DI Number

10851809002255

Quantity per Package

30

Contains DI Package

00851809002258

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box