Duns Number:627879687
Device Description: The VIA Procedure Kit custom includes transport pad, gauze, biohazard sticker, basin, lubr The VIA Procedure Kit custom includes transport pad, gauze, biohazard sticker, basin, lubricating jelly, gowns, Double-Header channel valve brush, BioGuard cleaning adapter, and Enzymatic sponge.
Catalog Number
00717373
Brand Name
VIA
Version/Model Number
00717373
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
-
Product Code
NWU
Product Code Name
Endoscope introducer kit
Public Device Record Key
f518206d-10df-44da-88f4-707ba751ec49
Public Version Date
February 04, 2022
Public Version Number
2
DI Record Publish Date
August 27, 2021
Package DI Number
10724995215849
Quantity per Package
12
Contains DI Package
00724995215842
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 51 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 902 |