Catalog Number

T20-121

Brand Name

De Soutter Medical

Version/Model Number

T20-121

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FQH

Product Code Name

Lavage, Jet

Public Device Record Key

c1f2e133-dcba-4d4b-94db-8f218f316bf5

Public Version Date

October 28, 2022

Public Version Number

2

DI Record Publish Date

October 10, 2022

Package DI Number

15051471179377

Quantity per Package

5

Contains DI Package

05051471179370

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box