Catalog Number

J9180

Brand Name

CLIP 9

Version/Model Number

J9180

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 01, 2016

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FZP

Product Code Name

Clip, Implantable

Public Device Record Key

f0eea45a-f825-4e41-84ca-3d6b3860daf1

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

September 17, 2015

Package DI Number

03661624006440

Quantity per Package

48

Contains DI Package

03661624004682

Package Discontinue Date

June 01, 2016

Package Status

Not in Commercial Distribution

Package Type

grouping carton