Catalog Number

IDDGLDGA

Brand Name

ID Glide

Version/Model Number

ID Glide 128 fl oz

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K051295,K051295

Product Code

NUC

Product Code Name

Lubricant, Personal

Public Device Record Key

526ba480-1804-4e51-b876-7694191282c9

Public Version Date

August 07, 2020

Public Version Number

5

DI Record Publish Date

January 23, 2017

Package DI Number

10761236101905

Quantity per Package

1

Contains DI Package

00761236101908

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case