Catalog Number

PH-51

Brand Name

ICU Medical

Version/Model Number

PH-51

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

K080989,K080989

Product Code

FMF

Product Code Name

Syringe, piston

Public Device Record Key

a710e0a6-b13f-4df8-ae1a-6e8972a32c45

Public Version Date

September 06, 2021

Public Version Number

1

DI Record Publish Date

August 29, 2021

Package DI Number

10887709092560

Quantity per Package

50

Contains DI Package

00887709092563

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS