Catalog Number

5200.X00V0

Brand Name

HJ® 3tlg. 20ML LL

Version/Model Number

5200.X00V0

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"

Yes

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

223b4946-3110-4535-8132-32f6b4fa6a15

Public Version Date

June 10, 2020

Public Version Number

1

DI Record Publish Date

June 02, 2020

Package DI Number

04035873063148

Quantity per Package

8

Contains DI Package

04035873063131

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CARTON