Catalog Number

-

Brand Name

Guardian Angel™ Rx

Version/Model Number

GA1000

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)

-

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

DQA

Product Code Name

Oximeter

Public Device Record Key

721509a6-5854-46e7-9fa4-8aac03b962e5

Public Version Date

April 10, 2019

Public Version Number

2

DI Record Publish Date

December 14, 2018

Package DI Number

14719872650017

Quantity per Package

1

Contains DI Package

04719872650010

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-