Duns Number:123407392
Device Description: SEDASYS DRUG DELIVERY CASSETTE
Catalog Number
SEDCAS01
Brand Name
SEDASYS
Version/Model Number
SEDCAS01
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 09, 2017
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
PDR
Product Code Name
Computer-assisted personalized sedation system
Public Device Record Key
534ed14f-7591-4dab-ae2e-9b69e62d73b8
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 17, 2014
Package DI Number
20705036003431
Quantity per Package
20
Contains DI Package
10705036003434
Package Discontinue Date
August 09, 2017
Package Status
Not in Commercial Distribution
Package Type
BOX
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 3 |
3 | A medical device with high risk that requires premarket approval | 16 |