Catalog Number

1100-607

Brand Name

BALFOUR RETRACTOR

Version/Model Number

1100-607

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

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FFO

Product Code Name

Retractor, Self-Retaining

Public Device Record Key

ee71bef7-894d-4b9f-8f48-189fdc36ce1a

Public Version Date

July 09, 2019

Public Version Number

2

DI Record Publish Date

June 18, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-