Duns Number:070556204
Device Description: Curaplex IV Start Kit w/Tegaderm, Alcohol Prep,2x2 Sponge,1 In Clear Tape,LF Tourniquet 1e Curaplex IV Start Kit w/Tegaderm, Alcohol Prep,2x2 Sponge,1 In Clear Tape,LF Tourniquet 1ea 50ea/cs
Catalog Number
670062-KIT
Brand Name
Curaplex
Version/Model Number
670062-KIT
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LRS
Product Code Name
I.V. start kit
Public Device Record Key
594fec3d-b95a-465e-9245-9f486b9f0044
Public Version Date
August 16, 2022
Public Version Number
3
DI Record Publish Date
December 15, 2018
Package DI Number
00810094570712
Quantity per Package
50
Contains DI Package
00815277029278
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CS
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 471 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 540 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 1 |