Duns Number:807613393
Device Description: 0.8 ml, 1.2% OVD Sodium Hyaluronate
Catalog Number
-
Brand Name
Ophthalin
Version/Model Number
6000080
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
P000046
Product Code
LZP
Product Code Name
Aid, Surgical, Viscoelastic
Public Device Record Key
8d572fbe-25e0-4ba7-88d9-0a3e1938060d
Public Version Date
January 06, 2022
Public Version Number
1
DI Record Publish Date
December 29, 2021
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 | 4 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 15 |
| 3 | A medical device with high risk that requires premarket approval | 15 |