Catalog Number

127100500

Brand Name

NA

Version/Model Number

1271-00-500

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 10, 2021

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

-

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

HRR

Product Code Name

SCISSORS, ORTHOPEDIC, SURGICAL

Public Device Record Key

0a767b6f-bae6-479b-b666-1e2e41376266

Public Version Date

September 23, 2022

Public Version Number

3

DI Record Publish Date

September 24, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-