Catalog Number

S-21082-M

Brand Name

Uline Wht 3 Mil Nitrile Glvs - M

Version/Model Number

S-21082-M

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

K952051,K952051,K952051

Product Code

LZA

Product Code Name

Polymer Patient Examination Glove

Public Device Record Key

42a4b1d4-2353-445a-bcd4-8f9ec48a0cc4

Public Version Date

June 19, 2020

Public Version Number

2

DI Record Publish Date

March 08, 2019

Package DI Number

30851253007299

Quantity per Package

10

Contains DI Package

10851253007295

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-