Catalog Number

-

Brand Name

DRIVEMEDICAL

Version/Model Number

HCANE-BK-C2

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

-

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

IPS

Product Code Name

CANE

Public Device Record Key

745ef87d-2753-44f6-8574-2b782f274a16

Public Version Date

July 16, 2019

Public Version Number

3

DI Record Publish Date

May 19, 2017

Package DI Number

10822383571031

Quantity per Package

24

Contains DI Package

50822383571039

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-