Duns Number:442126587
Catalog Number
-
Brand Name
RESERVOIR
Version/Model Number
D970 DIDECO AVANT R
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
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
K980600,K980600
Product Code
JOW
Product Code Name
SLEEVE, LIMB, COMPRESSIBLE
Public Device Record Key
d0e0ca1f-d3f1-4f60-b226-ad7b4cb46aa6
Public Version Date
January 22, 2020
Public Version Number
4
DI Record Publish Date
July 15, 2015
Package DI Number
38033178250284
Quantity per Package
6
Contains DI Package
08033178250283
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 25 |
2 | A medical device with a moderate to high risk that requires special controls. | 398 |
3 | A medical device with high risk that requires premarket approval | 78 |