Catalog Number

989805630111

Brand Name

PHILIPS

Version/Model Number

1080782

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

-

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

MNT

Product Code Name

Ventilator, continuous, minimal ventilatory support, facility use

Public Device Record Key

c1d0b4df-1cdd-4f13-9318-d7cd82e82bd4

Public Version Date

December 07, 2020

Public Version Number

2

DI Record Publish Date

September 22, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-