Duns Number:008018525
Device Description: 23 GA ULTRAVIT® Vitrectomy Probe
Catalog Number
-
Brand Name
CONSTELLATION® ULTRAVIT® ENGAUGE®
Version/Model Number
8065750949
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
MLZ
Product Code Name
Vitrectomy, instrument cutter
Public Device Record Key
f8034176-37c5-45bf-9024-7f2d4c59be1a
Public Version Date
January 24, 2022
Public Version Number
2
DI Record Publish Date
January 16, 2020
Package DI Number
10380657509499
Quantity per Package
6
Contains DI Package
00380657509492
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| 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 |