Catalog Number

VF-15232-E

Brand Name

ARROW

Version/Model Number

IPN001397

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K141051,K141051,K141051

Product Code

MSD

Product Code Name

Catheter, hemodialysis, implanted

Public Device Record Key

0245f3c3-b72e-4f22-8304-ad4b7213e19f

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

30801903128775

Quantity per Package

1

Contains DI Package

10801902128772

Package Discontinue Date

October 05, 2016

Package Status

Not in Commercial Distribution

Package Type

Box