CONAIR - Exfoliator - CONAIR CORPORATION

Duns Number:001661222

Device Description: Exfoliator

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More Product Details

Catalog Number

-

Brand Name

CONAIR

Version/Model Number

FCB3

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

GFE

Product Code Name

Brush, Dermabrasion, Powered

Device Record Status

Public Device Record Key

1a1a2591-e713-4706-b672-4ac9192b474d

Public Version Date

August 05, 2022

Public Version Number

1

DI Record Publish Date

July 28, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CONAIR CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 132
2 A medical device with a moderate to high risk that requires special controls. 62