Duns Number:790605856
Device Description: CS770 IntelliSpace Critical Care and Anesthesia Upgrade
Catalog Number
866148
Brand Name
IntelliSpace Critical Care and Anesthesia
Version/Model Number
CS770 IntelliSpace CC & Anesthesia Upgr
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
DXJ
Product Code Name
DISPLAY, CATHODE-RAY TUBE, MEDICAL
Public Device Record Key
fdadccbf-d4ce-4120-94f0-df473ec3cc5d
Public Version Date
February 16, 2022
Public Version Number
4
DI Record Publish Date
April 19, 2019
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 | 7 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 323 |
| 3 | A medical device with high risk that requires premarket approval | 36 |
| U | Unclassified | 1 |