Duns Number:196548481
Device Description: with High Flow Tip and Dual-Spike Adaptor
Catalog Number
0210-167-000
Brand Name
InterPulse
Version/Model Number
0210167000
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
f13a4646-b252-4e0b-be66-d5aa4fed2a72
Public Version Date
March 24, 2021
Public Version Number
5
DI Record Publish Date
September 23, 2016
Package DI Number
34546540861871
Quantity per Package
6
Contains DI Package
04546540861870
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
pack
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 2188 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3183 |
| U | Unclassified | 60 |