Catalog Number

SSD7 1240

Brand Name

Stephens Instruments

Version/Model Number

SSD7 1240

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

HNF

Product Code Name

SCISSORS, OPHTHALMIC

Public Device Record Key

c41c82f2-c619-4508-895d-45e76fa867b1

Public Version Date

October 01, 2020

Public Version Number

1

DI Record Publish Date

September 23, 2020

Package DI Number

00810799039866

Quantity per Package

10

Contains DI Package

00810799039873

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box