Catalog Number

2911

Brand Name

Tech-Med

Version/Model Number

2911

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K193259,K193259

Product Code

DXQ

Product Code Name

blood pressure cuff

Public Device Record Key

5f4198db-660c-4439-8aa0-982f5f182623

Public Version Date

May 23, 2022

Public Version Number

7

DI Record Publish Date

September 24, 2016

Package DI Number

20665973016973

Quantity per Package

100

Contains DI Package

10665973016976

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case