Duns Number:824793335
Catalog Number
-
Brand Name
ANTHONY GLASS ATOMIZER, CLEAR
Version/Model Number
S A163
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
-
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
ETF
Product Code Name
Unit, Examining/Treatment, Ent
Public Device Record Key
a5516f55-10a9-491b-817c-0af53b96f030
Public Version Date
September 28, 2021
Public Version Number
1
DI Record Publish Date
September 20, 2021
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 396 |