Catalog Number

SSD6 1050

Brand Name

Stephens Instruments

Version/Model Number

SSD6 1050

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

HXK

Product Code Name

HOLDER, NEEDLE; ORTHOPEDIC

Public Device Record Key

f1589e1c-0da8-4349-af76-6c85d1a2325f

Public Version Date

January 08, 2021

Public Version Number

2

DI Record Publish Date

September 23, 2020

Package DI Number

00810799039781

Quantity per Package

10

Contains DI Package

00810799039798

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box