Catalog Number
DECC055030
Brand Name
EliA Ro Well
Version/Model Number
DECC055030
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
K082759,K082759
Product Code
LKJ
Product Code Name
ANTINUCLEAR ANTIBODY, ANTIGEN, CONTROL
Public Device Record Key
c20755a3-4844-4e72-be7a-421f8f8a61c0
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 23, 2016
Package DI Number
07333066010588
Quantity per Package
4
Contains DI Package
07333066014548
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 225 |
2 | A medical device with a moderate to high risk that requires special controls. | 518 |