Duns Number:801895244
Device Description: IRRIJET® Single-Use WOUND IRRIGATION SYSTEM • SPLATTER-GARD AND 12 CC SYRINGE
Catalog Number
-
Brand Name
IRRIJET® Single-Use
Version/Model Number
55-2104
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
KYZ
Product Code Name
Syringe, Irrigating (Non Dental)
Public Device Record Key
219f726b-794e-43cd-93bb-2d22977f1cd3
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 14, 2017
Package DI Number
30888937015943
Quantity per Package
4
Contains DI Package
20888937015946
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 | 29 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1471 |
| 3 | A medical device with high risk that requires premarket approval | 2 |