Catalog Number

GDNPF102S

Brand Name

HandArmor

Version/Model Number

GDNPF102S

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

Yes

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

-

Product Code

LZA

Product Code Name

Polymer Patient Examination Glove

Public Device Record Key

4f01c572-ccda-4cf2-95fb-3803e188e587

Public Version Date

June 19, 2020

Public Version Number

2

DI Record Publish Date

April 02, 2020

Package DI Number

10787081122926

Quantity per Package

10

Contains DI Package

00787081122929

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box