Catalog Number

-

Brand Name

AED

Version/Model Number

ST1670

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 20, 2018

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

NWV

Product Code Name

Laparoscopic accessories, gynecologic

Public Device Record Key

c033df95-4e4e-4c3b-9a1c-fdba7a2fd37f

Public Version Date

December 21, 2018

Public Version Number

3

DI Record Publish Date

August 10, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-