Catalog Number

-

Brand Name

NIPRO DISPOSABLE SYRINGE

Version/Model Number

JD+03L2038-WEI

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

FMF

Product Code Name

Syringe, piston

Public Device Record Key

05488a23-3c77-4635-a379-726df18a3ab2

Public Version Date

September 12, 2018

Public Version Number

2

DI Record Publish Date

March 01, 2018

Package DI Number

10383790008300

Quantity per Package

100

Contains DI Package

00383790008303

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box