Catalog Number

-

Brand Name

ASA Techmed

Version/Model Number

AS-MC-PED

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K082542,K082542

Product Code

DXQ

Product Code Name

Blood Pressure Cuff

Public Device Record Key

e36a3254-6ce2-4ffa-b43f-1610e0e733b0

Public Version Date

January 04, 2019

Public Version Number

1

DI Record Publish Date

December 04, 2018

Package DI Number

26970366970034

Quantity per Package

50

Contains DI Package

06970366970030

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

MASTER CARTON