PHILIPS HeartStart OnSite - Guidelines Update, New HS1 - PHILIPS ELECTRONICS NORTH AMERICA CORPORATION

Duns Number:079503890

Device Description: Guidelines Update, New HS1

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

861334

Brand Name

PHILIPS HeartStart OnSite

Version/Model Number

861334

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

MKJ

Product Code Name

Automated External Defibrillators (Non-Wearable)

Device Record Status

Public Device Record Key

f1b08dff-9ea5-4bdf-ac67-2a3c340e32e6

Public Version Date

December 07, 2020

Public Version Number

4

DI Record Publish Date

September 24, 2014

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"PHILIPS ELECTRONICS NORTH AMERICA CORPORATION" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 14
3 A medical device with high risk that requires premarket approval 53