Catalog Number

448721

Brand Name

BD Phoenix™ NMIC/ID-121

Version/Model Number

448721

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"

-

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

K020322,K023444,K023634,K023858,K024153,K031429,K031530,K031699,K031912,K032153,K032275,K032299,K032567,K032655,K033458,K041384,K042932,K052269,K060214,K060217,K060257,K060444,K060447,K061327,K061355,K062944,K062945,K063301,K063573,K063811,K063824,K020322,K023444,K023634,K023858,K024153,K031429,K031530,K031699,K031912,K032153,K032275,K032299,K032567,K032655,K033458,K041384,K042932,K052269,K060214,K060217,K060257,K060444,K060447,K061327,K061355,K062944,K062945,K063301,K063573,K063811,K063824

Product Code

LON

Product Code Name

SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION

Public Device Record Key

9532549b-8385-42a6-8df6-23685af28a81

Public Version Date

November 08, 2018

Public Version Number

4

DI Record Publish Date

August 09, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-