Primary Device ID | 10801741018685 |
NIH Device Record Key | ffdfa5a5-31e5-4805-83e1-44990b800937 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProMax™ Series Bard® V-Max™ Roller Bar |
Version Model Number | 355404 |
Catalog Number | 355404 |
Company DUNS | 016898496 |
Company Name | C. R. Bard, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)526-4455 |
medical.services@crbard.com | |
Phone | +1(800)526-4455 |
medical.services@crbard.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741018688 [Primary] |
GS1 | 10801741018685 [Package] Contains: 00801741018688 Package: CA [5 Units] In Commercial Distribution |
FAS | ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-07-23 |
10801741018692 | ProMax™ Series Bard® V-Max™ Roller Bar, Resectoscope Compatibility: Storz Single Stem 24 Fr |
10801741018685 | ProMax™ Series Bard® V-Max™ Roller Bar, Resectoscope Compatibility: Storz Double Stem 24 Fr |
10801741018678 | ProMax™ Series Bard® V-Max™ Roller Bar, Resectoscope Compatibility: Olympus OES 24 Fr. |
10801741018661 | ProMax™ Series Bard® V-Max™ Roller Bar, Resectoscope Compatibility: ACMI Classic Series 24 |
10801741018654 | ProMax™ Series Bard® V-Max™ Roller Bar, Resectoscope Compatibility: ACMI USA Series 24 Fr. |