Catalog Number

BD 111

Brand Name

SteriTec Steri-Pak LF Bowie-Dick Test Pack

Version/Model Number

BD 111

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

JOJ

Product Code Name

Indicator, Physical/Chemical Sterilization Process

Public Device Record Key

25ddf8ea-41fe-4204-a8c9-78bbcfab0dda

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

10814434020018

Quantity per Package

20

Contains DI Package

00814434020011

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case