Catalog Number

-

Brand Name

MicroFrance®

Version/Model Number

8820

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 26, 2019

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

ERA

Product Code Name

OTOSCOPE

Public Device Record Key

c0981e08-a94c-44cb-a76e-d53087b3d167

Public Version Date

December 06, 2019

Public Version Number

4

DI Record Publish Date

June 02, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-