Catalog Number

PH36TTTHB

Brand Name

CARDINAL HEALTH

Version/Model Number

PH36TTTHB

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)

Yes

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

GCX

Product Code Name

APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED

Public Device Record Key

9f2f0088-14b1-4748-a070-c79ba6881702

Public Version Date

June 17, 2022

Public Version Number

2

DI Record Publish Date

January 20, 2022

Package DI Number

50195594133625

Quantity per Package

1

Contains DI Package

10195594133627

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE