Catalog Number

460970462

Brand Name

Transpac™

Version/Model Number

460970462

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K052828,K052828

Product Code

DRS

Product Code Name

Transducer, blood-pressure, extravascular

Public Device Record Key

2b2c4f54-7817-4c8b-9502-e55b0a3d2e8d

Public Version Date

August 05, 2021

Public Version Number

1

DI Record Publish Date

July 28, 2021

Package DI Number

10840619063280

Quantity per Package

20

Contains DI Package

00840619063283

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS