Catalog Number

-

Brand Name

Sarns™ Infusion Line

Version/Model Number

16110

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

K810079,K810079

Product Code

KRI

Product Code Name

Accessory Equipment, Cardiopulmonary Bypass

Public Device Record Key

90e1afd7-e3a3-4df1-82a2-7d419b92ecd0

Public Version Date

October 19, 2021

Public Version Number

4

DI Record Publish Date

October 02, 2015

Package DI Number

50699753001942

Quantity per Package

3

Contains DI Package

00699753001947

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

3 Piece Case