Duns Number:015623119
Catalog Number
MAMC213-08
Brand Name
Halyard
Version/Model Number
MAMC213-08_0017
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
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OGD
Product Code Name
Custom anesthesia tray
Public Device Record Key
44ff547f-8c45-4ab2-8be2-d1435daed811
Public Version Date
June 16, 2022
Public Version Number
1
DI Record Publish Date
June 08, 2022
Package DI Number
20809160372743
Quantity per Package
20
Contains DI Package
10809160372746
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 | 5180 |
2 | A medical device with a moderate to high risk that requires special controls. | 28744 |