Duns Number:103021940
Device Description: VITREOUS CUTTER, 25G, HIGH SPEED(6 PACK)
Catalog Number
NGP0025
Brand Name
DISPOSABLE 25GA VITRECTOMY CUTTER
Version/Model Number
NGP0025
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
MLZ
Product Code Name
VITRECTOMY, INSTRUMENT CUTTER
Public Device Record Key
a1bcaf78-dcfa-4bf9-bf51-bf2d2cfb026a
Public Version Date
February 26, 2020
Public Version Number
4
DI Record Publish Date
September 02, 2016
Package DI Number
15050474534114
Quantity per Package
6
Contains DI Package
05050474534117
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 | 42 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 77 |
| 3 | A medical device with high risk that requires premarket approval | 3950 |