Restylane Lyft with Lidocaine - Q-Med AB

Duns Number:355371873

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

-

Brand Name

Restylane Lyft with Lidocaine

Version/Model Number

Gel 1 mL - Demo

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

P040024

Product Code Details

Product Code

LMH

Product Code Name

Implant, Dermal, For Aesthetic Use

Device Record Status

Public Device Record Key

50525752-54cc-4fab-bad4-c1ffbcf396b4

Public Version Date

March 09, 2021

Public Version Number

1

DI Record Publish Date

March 01, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"Q-MED AB" Characteristics
Device Class Device Class Description No of Devices
3 A medical device with high risk that requires premarket approval 35