Cellfina Motor Module Device and Package - EU part should not have been registered with GUDID - ULTHERA, INC.

Duns Number:010981554

Device Description: EU part should not have been registered with GUDID

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More Product Details

Catalog Number

-

Brand Name

Cellfina Motor Module Device and Package

Version/Model Number

CM1-EU Rev A

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 07, 2016

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

K153677

Product Code Details

Product Code

OUP

Product Code Name

Powered Surgical Instrument For Improvement In The Appearance Of Cellulite

Device Record Status

Public Device Record Key

be69ab63-cb5f-481c-b00c-6a4b10ff6bc8

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

December 14, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ULTHERA, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 63