Duns Number:060467826
Device Description: LYFO DISK™ E. coli CDC AR-0346
Catalog Number
01259L
Brand Name
LYFO DISK™
Version/Model Number
01259L
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
JTR
Product Code Name
KIT, QUALITY CONTROL FOR CULTURE MEDIA
Public Device Record Key
331cba26-ac97-465b-8aa7-74b08c0c0987
Public Version Date
May 08, 2020
Public Version Number
1
DI Record Publish Date
April 30, 2020
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 | 1104 |
2 | A medical device with a moderate to high risk that requires special controls. | 24 |