Catalog Number

UR203

Brand Name

Uresta®

Version/Model Number

UR203

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K083769,K083769

Product Code

HHW

Product Code Name

Pessary, Vaginal

Public Device Record Key

846d13dd-c814-4a1e-bc52-c0ce4e72d33d

Public Version Date

March 10, 2021

Public Version Number

3

DI Record Publish Date

November 23, 2020

Package DI Number

10692379000216

Quantity per Package

12

Contains DI Package

00692379000219

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-