Catalog Number

03-2622-3

Brand Name

CombiSet

Version/Model Number

03-2622-3

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

K962081,K962081

Product Code

FJK

Product Code Name

SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE

Public Device Record Key

2b0fae5e-35fc-4810-b12f-195bbedc4e20

Public Version Date

June 07, 2019

Public Version Number

4

DI Record Publish Date

September 24, 2015

Package DI Number

10840861100238

Quantity per Package

24

Contains DI Package

00840861100231

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-