Duns Number:008124539
Device Description: Sterile Nitrile Examination Glove, Cuffed and Powder-Free, Ambidextrous, 1 Glove per Packa Sterile Nitrile Examination Glove, Cuffed and Powder-Free, Ambidextrous, 1 Glove per Package, Small
Catalog Number
-
Brand Name
Sterile Nitrile Examination Glove
Version/Model Number
6522
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
f4d514f2-f8fe-4e22-b226-021cfa66c16e
Public Version Date
May 02, 2022
Public Version Number
1
DI Record Publish Date
April 22, 2022
Package DI Number
00616784652221
Quantity per Package
100
Contains DI Package
00616784652214
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 694 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 226 |
| 3 | A medical device with high risk that requires premarket approval | 2 |