Catalog Number

JLL-IN 00 01-N

Brand Name

JULIET ® INSTRUMENTATION

Version/Model Number

JLL-IN 00 01-N

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 30, 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

GDI

Product Code Name

Dissector, Surgical, General & Plastic Surgery

Public Device Record Key

1cfd9e1b-ee9b-4c07-ac8d-7c131bfe803a

Public Version Date

December 05, 2018

Public Version Number

2

DI Record Publish Date

July 30, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-