Catalog Number

R9180

Brand Name

CLIP 9 VITALITEC

Version/Model Number

R9180

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

451daa31-cafc-4585-8a9f-9bd8e2cc6503

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

July 31, 2019

Package DI Number

13661522039943

Quantity per Package

20

Contains DI Package

03661522039946

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-