Catalog Number

-

Brand Name

Techniglove International

Version/Model Number

STN205P

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)

-

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

422a4404-7494-4752-869c-af56c2eed3f9

Public Version Date

June 19, 2020

Public Version Number

2

DI Record Publish Date

December 27, 2019

Package DI Number

00850008325465

Quantity per Package

4

Contains DI Package

10850008325455

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case