Catalog Number

-

Brand Name

NIPRO DISPOSABLE SYRINGE

Version/Model Number

JD+05L2238-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

f3a1c7d1-8926-4813-af5e-c000fb74252e

Public Version Date

September 12, 2018

Public Version Number

2

DI Record Publish Date

March 01, 2018

Package DI Number

40383790008721

Quantity per Package

12

Contains DI Package

10383790008720

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case