Duns Number:003080678
Device Description: CaviWipesXL 10” x 12” 50 Individual Packets/Box
Catalog Number
691155
Brand Name
Hopkins Medical Products®
Version/Model Number
691155
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
-
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
LRJ
Product Code Name
Disinfectant, medical devices
Public Device Record Key
f205b551-5d82-47eb-8a0d-2025313191db
Public Version Date
May 23, 2019
Public Version Number
2
DI Record Publish Date
September 28, 2018
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 96 |
2 | A medical device with a moderate to high risk that requires special controls. | 135 |