Catalog Number

-

Brand Name

MINT

Version/Model Number

MINT lift ML 1043

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

Yes

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

NEW

Product Code Name

Suture, Surgical, Absorbable, Polydioxanone

Public Device Record Key

ed62aa59-7244-4b29-b459-1b07e27e2f73

Public Version Date

January 03, 2022

Public Version Number

2

DI Record Publish Date

November 25, 2021

Package DI Number

18809556174451

Quantity per Package

5

Contains DI Package

08809556174454

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box Package