Catalog Number

5701883

Brand Name

Henry Schein

Version/Model Number

5701883

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

FNY

Product Code Name

BASIN, EMESIS

Public Device Record Key

5ce77342-fdb7-4fea-a6b2-dca6a04a7650

Public Version Date

May 03, 2021

Public Version Number

1

DI Record Publish Date

April 23, 2021

Package DI Number

30304040127866

Quantity per Package

10

Contains DI Package

20304040127869

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case