Catalog Number

EJM1008

Brand Name

Jamshidi

Version/Model Number

EJM1008

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

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

KNW

Product Code Name

INSTRUMENT, BIOPSY

Public Device Record Key

3cdfc51c-de20-4657-8056-4ad182411f78

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 02, 2017

Package DI Number

50885403464209

Quantity per Package

10

Contains DI Package

10885403464201

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case