Catalog Number

750216

Brand Name

Anchor

Version/Model Number

1

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 05, 2022

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

22818f29-08c0-4303-acbe-9cec70ffa4a4

Public Version Date

October 06, 2022

Public Version Number

2

DI Record Publish Date

May 04, 2020

Package DI Number

00813360021314

Quantity per Package

144

Contains DI Package

00813360023059

Package Discontinue Date

October 05, 2022

Package Status

Not in Commercial Distribution

Package Type

case