Duns Number:790265227
Device Description: 23 Gauge Vitreous Cutter, R1, w/ 79"/98” MID Labs Tubing Set, Sterile, Single Use
Catalog Number
2520CE
Brand Name
NA
Version/Model Number
2520CE
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
-
Product Code
HQE
Product Code Name
Instrument, Vitreous Aspiration And Cutting, Ac-Powered
Public Device Record Key
b64c39e1-24cd-4b62-8aaf-7d2a4ce93376
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 23, 2016
Package DI Number
10812480010120
Quantity per Package
6
Contains DI Package
00812480010123
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 9 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 30 |