Duns Number:070556204
Device Description: Curaplex First Call In Bag, Contents Only Latex Free
Catalog Number
FCB-CLF
Brand Name
Curaplex
Version/Model Number
FCB-CLF
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
OHO
Product Code Name
First aid kit without drug
Public Device Record Key
135bf958-d283-49fe-96c2-2dd0c13d5d88
Public Version Date
August 16, 2022
Public Version Number
3
DI Record Publish Date
December 18, 2017
Package DI Number
00810094573492
Quantity per Package
10
Contains DI Package
00817617029139
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 |