Catalog Number

-

Brand Name

HandyTube™

Version/Model Number

3711015

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

IKX

Product Code Name

AID, TRANSFER

Public Device Record Key

bacff0aa-f08e-4b4f-b7e1-30c91d13f74e

Public Version Date

October 19, 2021

Public Version Number

2

DI Record Publish Date

March 23, 2021

Package DI Number

10887761979618

Quantity per Package

10

Contains DI Package

00887761979611

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-