Catalog Number

-

Brand Name

UNBRANDED

Version/Model Number

08-CC160-UBA

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"

Yes

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

K012168,K012168

Product Code

KKX

Product Code Name

Drape, surgical

Public Device Record Key

45ced1ed-b9fa-4042-a303-a37a2e4a0054

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 07, 2016

Package DI Number

10848340008853

Quantity per Package

10

Contains DI Package

00848340008856

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-