Catalog Number

WSP30-00-S/3

Brand Name

Ambu WhiteSensor WSP30

Version/Model Number

WSP30-00-S/3

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 10, 2020

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

-

Product Code

DRX

Product Code Name

Electrode, electrocardiograph

Public Device Record Key

273fe55c-22f0-480d-86f9-0a626f8f9dc0

Public Version Date

September 10, 2020

Public Version Number

2

DI Record Publish Date

June 03, 2019

Package DI Number

05707480141371

Quantity per Package

200

Contains DI Package

05707480141364

Package Discontinue Date

September 10, 2020

Package Status

Not in Commercial Distribution

Package Type

-