Catalog Number

SID35GWBLA

Brand Name

CARDINAL HEALTH

Version/Model Number

SID35GWBLA

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

-

Product Code

FNY

Product Code Name

BASIN, EMESIS

Public Device Record Key

692ded88-fd9d-4bec-bd4c-4d2790903d8e

Public Version Date

June 17, 2022

Public Version Number

6

DI Record Publish Date

August 03, 2016

Package DI Number

50885425413483

Quantity per Package

20

Contains DI Package

10885425413485

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE