Catalog Number

SA250

Brand Name

ICU Medical

Version/Model Number

SA250

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

K923966,K923966

Product Code

LHI

Product Code Name

Set, i.V. Fluid transfer

Public Device Record Key

0a684a23-0f94-49c0-89df-926c3b879481

Public Version Date

September 06, 2021

Public Version Number

1

DI Record Publish Date

August 29, 2021

Package DI Number

10887709080314

Quantity per Package

250

Contains DI Package

00887709080317

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS