Duns Number:070556204
Device Description: *Custom* Detroit PD IFAK
Catalog Number
8600-01450
Brand Name
Curaplex
Version/Model Number
8600-01450
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
ea430c0b-470e-48c6-b6ca-3ca4274877cd
Public Version Date
August 16, 2022
Public Version Number
2
DI Record Publish Date
April 30, 2020
Package DI Number
00810094571597
Quantity per Package
20
Contains DI Package
00812277036305
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 |