Catalog Number

-

Brand Name

BTAVAL

Version/Model Number

070436808

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

-

Product Code

KCT

Product Code Name

Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Public Device Record Key

0416d956-2e0e-4794-bda2-c8a09baed846

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

D6620704368084

Quantity per Package

6

Contains DI Package

D6620704368082

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE