Duns Number:109903521
Device Description: POWERPULSE LAVAGE HIP/KNEE DISPOSABLE UNIT WITHOUT SUCT POWERPULSE LAVAGE HIP/KNEE DISPOSABLE UNIT WITHOUT SUCTION
Catalog Number
71277005
Brand Name
POWERPULSE
Version/Model Number
71277005
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
FQH
Product Code Name
LAVAGE, JET
Public Device Record Key
0d6171f9-1f25-4d28-ba2f-1270f6564362
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 29, 2015
Package DI Number
23596010421306
Quantity per Package
10
Contains DI Package
03596010421302
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 10651 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 35590 |
| 3 | A medical device with high risk that requires premarket approval | 351 |