Catalog Number

-

Brand Name

E6518 Bag Heavy Duty PE Film 48x38cm

Version/Model Number

E6518

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KKX

Product Code Name

Drape, Surgical

Public Device Record Key

fc85234c-8739-4791-9860-9a1327ba6eea

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 27, 2016

Package DI Number

00816953029728

Quantity per Package

120

Contains DI Package

00816953029711

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case