Duns Number:134139174
Device Description: EV1000 PLATFORM
Catalog Number
EV1000A
Brand Name
EV1000
Version/Model Number
EV1000A
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
DSB
Product Code Name
Plethysmograph, Impedance
Public Device Record Key
ef2665a9-a955-4e6a-a170-ad1c6939b6b9
Public Version Date
November 10, 2021
Public Version Number
8
DI Record Publish Date
September 03, 2016
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 | 5 |
2 | A medical device with a moderate to high risk that requires special controls. | 643 |
3 | A medical device with high risk that requires premarket approval | 212 |