Duns Number:354019424
Device Description: EliA M2 Positive Control 2500/5000
Catalog Number
83-0015-01
Brand Name
EliA M2 Positive Control 2500/5000
Version/Model Number
83-0015-01
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
K181556,K181556
Product Code
DBM
Product Code Name
ANTIMITOCHONDRIAL ANTIBODY, INDIRECT IMMUNOFLUORESCENT, ANTIGEN, CONTROL
Public Device Record Key
5a8c9dee-98ed-49aa-a4cb-ceaf2a76030a
Public Version Date
December 17, 2020
Public Version Number
1
DI Record Publish Date
December 09, 2020
Package DI Number
07333066014333
Quantity per Package
6
Contains DI Package
07333066013527
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 |