Duns Number:012430880
Device Description: One Step iFOBT Return Mailers
Catalog Number
9004416
Brand Name
Henry Schein
Version/Model Number
9004416
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
KHE
Product Code Name
REAGENT, OCCULT BLOOD
Public Device Record Key
02667ef8-21c2-4a04-b783-a04b2d6e98bd
Public Version Date
April 08, 2022
Public Version Number
7
DI Record Publish Date
September 24, 2016
Package DI Number
10304040002565
Quantity per Package
8
Contains DI Package
00304040002568
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 3829 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2579 |
| 3 | A medical device with high risk that requires premarket approval | 1 |
| U | Unclassified | 34 |