Catalog Number

-

Brand Name

DK50 DE

Version/Model Number

STA NOZ 230V/50Hz 3,5bar WALL NO

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 29, 2016

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

BTI

Product Code Name

Compressor, Air, Portable

Public Device Record Key

1ac2141e-6235-40fa-bdae-e3c86ea1a5fa

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 29, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-