Catalog Number

TF33630

Brand Name

Transfix Continence Sheath

Version/Model Number

TF33630

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"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NNX

Product Code Name

DEVICE, INCONTINENCE, UROSHEATH TYPE, NON-STERILE

Public Device Record Key

5aea0bfa-7917-4494-b393-d745c0849ea6

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

September 22, 2020

Package DI Number

10801741072373

Quantity per Package

30

Contains DI Package

00801741072376

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA