Duns Number:131747628
Device Description: VISCOUS SPRAY II
Catalog Number
ABS-10052
Brand Name
Arthrex®
Version/Model Number
ABS-10052
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 27, 2020
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"
Yes
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
-
Product Code
KYZ
Product Code Name
SYRINGE, IRRIGATING (NON DENTAL)
Public Device Record Key
92b8eef6-46f4-43f5-a41c-6f7b344afde0
Public Version Date
January 28, 2020
Public Version Number
5
DI Record Publish Date
February 15, 2017
Package DI Number
10888867001982
Quantity per Package
5
Contains DI Package
00888867001985
Package Discontinue Date
January 27, 2020
Package Status
Not 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 | 6506 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3411 |
| 3 | A medical device with high risk that requires premarket approval | 1 |
| U | Unclassified | 2 |