Duns Number:008018525
Device Description: Alcon Intrepid 0.3mm Polymer I/A Bimanual Set
Catalog Number
-
Brand Name
Alcon, Intrepid
Version/Model Number
8065751922
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"
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
HQC
Product Code Name
Unit, phacofragmentation
Public Device Record Key
1a0be5d5-e3d1-4eee-979b-0c883423c65e
Public Version Date
October 07, 2019
Public Version Number
6
DI Record Publish Date
September 24, 2016
Package DI Number
10380657519221
Quantity per Package
6
Contains DI Package
00380657519224
Package Discontinue Date
-
Package Status
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 | 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 |