Primary Device ID | 10801741098038 |
NIH Device Record Key | c83511e2-84aa-4ff8-b0ae-9360ea4e4f07 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HydroSil Go™ Intermittent Urinary Catheter |
Version Model Number | 71816 |
Catalog Number | 71816 |
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 | true |
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 |
Catheter Gauge | 16 French |
Catheter Gauge | 16 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741098031 [Primary] |
GS1 | 10801741098038 [Package] Contains: 00801741098031 Package: CA [30 Units] In Commercial Distribution |
EZD | CATHETER, STRAIGHT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-12-08 |
10801741098052 | HydroSil Go® Intermittent Urinary Catheter |
10801741098038 | HydroSil Go® Intermittent Urinary Catheter |
10801741098014 | HydroSil Go® Intermittent Urinary Catheter |
10801741097994 | HydroSil Go® Intermittent Urinary Catheter |
10801741097970 | HydroSil Go® Intermittent Urinary Catheter |
10801741097956 | HydroSil Go™ Intermittent Urinary Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HYDROSIL GO 86350771 not registered Dead/Abandoned |
Rochester Medical Corporation 2014-07-29 |