Catalog Number

-

Brand Name

SLS-CLIP

Version/Model Number

V3120-1

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

e9c0fbcc-5bce-4d1e-906d-883b909a9807

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

September 17, 2015

Package DI Number

3661624006419

Quantity per Package

48

Contains DI Package

03661624000202

Package Discontinue Date

June 01, 2016

Package Status

Not in Commercial Distribution

Package Type

grouping carton