Catalog Number

-

Brand Name

hypodermic syringes(safety needle)

Version/Model Number

1ml 23G×25mmTW

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)

-

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

da0b9cb2-64c9-422a-bedf-ce3733d79688

Public Version Date

March 08, 2021

Public Version Number

1

DI Record Publish Date

February 26, 2021

Package DI Number

06949236205183

Quantity per Package

100

Contains DI Package

06949236205176

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-