Catalog Number

-

Brand Name

MediSourceNet, Inc

Version/Model Number

WELF

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K192035,K192035

Product Code

FYD

Product Code Name

Apparatus, Exhaust, Surgical

Public Device Record Key

d125bd9c-e6d5-4bf5-b8a6-25fbb0b3a315

Public Version Date

September 07, 2021

Public Version Number

1

DI Record Publish Date

August 30, 2021

Package DI Number

10850034735129

Quantity per Package

20

Contains DI Package

00850034735122

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case