Duns Number:005083209
Device Description: Admix Dispensing Pin
Catalog Number
H93849
Brand Name
NA
Version/Model Number
H93849
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"
Yes
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
K872743,K900585,K872743,K900585
Product Code
FMF
Product Code Name
Syringe, piston
Public Device Record Key
fcebb566-9ee3-415d-9b07-4c5f3ed03782
Public Version Date
February 19, 2021
Public Version Number
5
DI Record Publish Date
September 23, 2016
Package DI Number
55413765482590
Quantity per Package
50
Contains DI Package
05413765482595
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 16 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 101 |
| 3 | A medical device with high risk that requires premarket approval | 19 |