Catalog Number

418027

Brand Name

Replacement Cap

Version/Model Number

418027

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

f0a2e0e1-3007-4a99-abc3-61173c0e3415

Public Version Date

October 07, 2020

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

04046964183416

Quantity per Package

10

Contains DI Package

04046964183409

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton