Duns Number:217207083
Device Description: ADULT RIGHT ANKLE CUFF
Catalog Number
ACC-VAS-024
Brand Name
DOPPLEX
Version/Model Number
ACC-VAS-024
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
K121108
Product Code
JOM
Product Code Name
Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Public Device Record Key
eb9ed733-cbf6-48ad-858a-c48d39e61f22
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 12, 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 159 |