Catalog Number

30-8179E

Brand Name

CARDINAL HEALTH

Version/Model Number

30-8179E

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

GCX

Product Code Name

APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED

Public Device Record Key

0dc4958d-b3a8-4802-9950-9a8738df68bb

Public Version Date

June 17, 2022

Public Version Number

4

DI Record Publish Date

March 22, 2018

Package DI Number

50887488946410

Quantity per Package

40

Contains DI Package

10887488946412

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE