Catalog Number

U-HCG-101

Brand Name

UCP Home

Version/Model Number

U-HCG-101

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LCX

Product Code Name

Kit, Test, Pregnancy, Hcg, Over The Counter

Public Device Record Key

a3aa98f6-8e51-47da-89ba-cf826842ec8e

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

December 05, 2016

Package DI Number

20817038021266

Quantity per Package

40

Contains DI Package

10817038021269

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case