Duns Number:008018525
Device Description: OPTI-FREE PUREMOIST Pro Rewetting Drops 12ml
Catalog Number
-
Brand Name
OPTI-FREE PUREMOIST
Version/Model Number
OPTI-FREE PUREMOIST 12ml
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)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LPN
Product Code Name
Accessories, soft lens products
Public Device Record Key
92f0813c-6d11-4332-996f-ecaafc547d6d
Public Version Date
January 24, 2022
Public Version Number
4
DI Record Publish Date
September 24, 2016
Package DI Number
20300650192372
Quantity per Package
24
Contains DI Package
00300650192378
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 | 250 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 541 |
| 3 | A medical device with high risk that requires premarket approval | 6098 |