Catalog Number

-

Brand Name

AD Surgical

Version/Model Number

A400-HFD

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

PUI

Product Code Name

Drape, Surgical, Exempt

Public Device Record Key

48c3b639-ed27-4dc2-ba5d-7f9f6585b5b8

Public Version Date

June 22, 2021

Public Version Number

3

DI Record Publish Date

January 15, 2021

Package DI Number

10814639022060

Quantity per Package

10

Contains DI Package

00814639022063

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box