Catalog Number

-

Brand Name

Antmed

Version/Model Number

PT111103

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

K091408,K091408

Product Code

DRS

Product Code Name

Transducer, Blood-Pressure, Extravascular

Public Device Record Key

5b3353b1-bf0c-4aa1-b534-4f3fd8d02958

Public Version Date

October 31, 2018

Public Version Number

5

DI Record Publish Date

August 24, 2017

Package DI Number

06945764404036

Quantity per Package

30

Contains DI Package

06945764400212

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-