Catalog Number

-

Brand Name

MicroAire®

Version/Model Number

7000-020

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 30, 2021

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

HSZ

Product Code Name

Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment

Public Device Record Key

7b792e9f-db9e-4926-9147-c0a85bf86796

Public Version Date

July 04, 2022

Public Version Number

3

DI Record Publish Date

December 29, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-