Duns Number:201179681
Catalog Number
-
Brand Name
TUBE, CAPILLARY, VETERINARY, (BUNDLE 50)
Version/Model Number
AT-0007-00-00
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 02, 2020
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
-
Product Code Name
-
Public Device Record Key
5b9e8b9e-55db-4857-9b6b-931660713cfc
Public Version Date
August 05, 2022
Public Version Number
5
DI Record Publish Date
August 17, 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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 25 |