Duns Number:025460908
Device Description: NEOB GLOVE PACK 6.5 (15 PR)
Catalog Number
DYNJ55044
Brand Name
Medline Industries, Inc.
Version/Model Number
DYNJ55044
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K093726,K093726
Product Code
LZA
Product Code Name
Polymer patient examination glove
Public Device Record Key
4ace027e-5762-4292-a655-26463e7cb0d5
Public Version Date
June 17, 2022
Public Version Number
5
DI Record Publish Date
August 28, 2018
Package DI Number
40889942529361
Quantity per Package
25
Contains DI Package
10889942529360
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 38540 |
2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
3 | A medical device with high risk that requires premarket approval | 2 |
U | Unclassified | 7 |