Beurer - Light based, over the counter device intended for - BEURER NORTH AMERICA, L.P.

Duns Number:078497467

Device Description: Light based, over the counter device intended for the removal of unwanted hair as well as Light based, over the counter device intended for the removal of unwanted hair as well as permanent reduction in hair regrowth.

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More Product Details

Catalog Number

-

Brand Name

Beurer

Version/Model Number

IPL7500 (Art.-No. 575.71)

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

OHT

Product Code Name

Light Based Over-The-Counter Hair Removal

Device Record Status

Public Device Record Key

b5c80362-0474-43a4-9c91-173a8ed2be84

Public Version Date

October 19, 2021

Public Version Number

4

DI Record Publish Date

June 12, 2017

Additional Identifiers

Package DI Number

10852547004730

Quantity per Package

2

Contains DI Package

00852547004733

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case Pack

"BEURER NORTH AMERICA, L.P." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 7
2 A medical device with a moderate to high risk that requires special controls. 90
U Unclassified 2