Duns Number:016898496
Device Description: ProMax™ Series Bard® V-Max™ Roller Bar, Resectoscope Compatibility: ACMI Classic Series 24 ProMax™ Series Bard® V-Max™ Roller Bar, Resectoscope Compatibility: ACMI Classic Series 24 Fr.
Catalog Number
355402
Brand Name
ProMax™ Series Bard® V-Max™ Roller Bar
Version/Model Number
355402
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
FAS
Product Code Name
ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL
Public Device Record Key
ec2e636d-73c7-4687-b0c8-60e7504e255d
Public Version Date
February 07, 2019
Public Version Number
4
DI Record Publish Date
July 23, 2016
Package DI Number
10801741018661
Quantity per Package
5
Contains DI Package
00801741018664
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CA
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 472 |
2 | A medical device with a moderate to high risk that requires special controls. | 1994 |
U | Unclassified | 10 |