Catalog Number

-

Brand Name

Custom Healthcare Systems Inc.

Version/Model Number

D20-11250

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)

Yes

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

-

Product Code

FQM

Product Code Name

Bandage, Elastic

Public Device Record Key

e33c56a8-c5df-422d-9f35-6eb5942bbc0d

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

July 29, 2018

Package DI Number

20811870032534

Quantity per Package

100

Contains DI Package

00811870032530

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

N/A