Catalog Number

-

Brand Name

ID Velvet

Version/Model Number

ID Velvet 2 ml Foil

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

-

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

NUC

Product Code Name

Lubricant, Personal

Public Device Record Key

9320ff40-2585-4d8f-80bd-1425c09f473a

Public Version Date

August 07, 2020

Public Version Number

3

DI Record Publish Date

March 06, 2018

Package DI Number

00761236110153

Quantity per Package

144

Contains DI Package

00761236110146

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Bag