Catalog Number

-

Brand Name

AHS

Version/Model Number

AH03S2219

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

fe37668e-5a7d-4b69-922b-41f4ae3d360a

Public Version Date

November 09, 2020

Public Version Number

5

DI Record Publish Date

March 31, 2016

Package DI Number

B031AH03S22192

Quantity per Package

2000

Contains DI Package

B031AH03S22191

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton