Catalog Number

-

Brand Name

BV Medical

Version/Model Number

20-207-015-L

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

DXQ

Product Code Name

Blood Pressure Cuff

Public Device Record Key

d4a9387b-ef61-4e1f-9b85-ec936183984d

Public Version Date

January 28, 2019

Public Version Number

5

DI Record Publish Date

December 16, 2016

Package DI Number

00845821028136

Quantity per Package

24

Contains DI Package

00845821001474

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-