Catalog Number

-

Brand Name

Strauss Surgical

Version/Model Number

STS-5135-320HA

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

FGA

Product Code Name

Kit, Nephroscope

Public Device Record Key

0052a0e2-c5a5-4e91-a3db-86b18830b862

Public Version Date

April 29, 2020

Public Version Number

2

DI Record Publish Date

December 19, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-