Catalog Number

750233

Brand Name

Anchor

Version/Model Number

1001

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

GEC

Product Code Name

Brush, Scrub, Operating-Room

Public Device Record Key

332256c3-80c3-48a4-9cf9-811dc51074d9

Public Version Date

October 13, 2022

Public Version Number

1

DI Record Publish Date

October 05, 2022

Package DI Number

10813360023292

Quantity per Package

12

Contains DI Package

00813360023295

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Pack