Catalog Number

515203

Brand Name

BD PhaSeal

Version/Model Number

515203

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

LHI

Product Code Name

Set, i.V. Fluid transfer

Public Device Record Key

f642fb93-8528-479a-afbb-28524d551781

Public Version Date

October 23, 2019

Public Version Number

5

DI Record Publish Date

September 19, 2016

Package DI Number

50382905152035

Quantity per Package

4

Contains DI Package

30382905152031

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case