Catalog Number

-

Brand Name

Home Green Leaf

Version/Model Number

C2050S

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LZA

Product Code Name

Polymer Patient Examination Glove

Public Device Record Key

89169e47-9512-4f3f-95a5-c7fbe646034e

Public Version Date

June 19, 2020

Public Version Number

2

DI Record Publish Date

June 17, 2019

Package DI Number

00608106000711

Quantity per Package

10

Contains DI Package

00608106000704

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case