Duns Number:092519016
Device Description: Volatiles (WB) 2-Part
Catalog Number
99119
Brand Name
Volatiles (WB) 2-Part
Version/Model Number
99119
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
-
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
LAS
Product Code Name
Drug Specific Control Materials
Public Device Record Key
d4e3e1b1-90b9-4786-a0e6-9645e818a00a
Public Version Date
April 23, 2020
Public Version Number
1
DI Record Publish Date
April 15, 2020
Package DI Number
B800991195
Quantity per Package
5
Contains DI Package
B800991190
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 113 |