| Primary Device ID | 10610075101990 | 
| NIH Device Record Key | 43920853-1e44-4f0e-a150-0cc7e2b06c44 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Advance Plus | 
| Version Model Number | 94164IC | 
| Company DUNS | 005527098 | 
| Company Name | HOLLISTER INCORPORATED | 
| Device Count | 25 | 
| 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)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | |
| Phone | +1(800)323-4060 | 
| cs@hollister.com | 
| Catheter Gauge | 16 French | 
| Catheter Gauge | 16 French | 
| Catheter Gauge | 16 French | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Length | 16 Inch | 
| Catheter Gauge | 16 French | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00610075101993 [Primary] | 
| GS1 | 10610075101990 [Package] Contains: 00610075101993 Package: Case [4 Units] In Commercial Distribution | 
| GS1 | 30610075101994 [Unit of Use] | 
| KOD | CATHETER, UROLOGICAL | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-12-03 | 
| Device Publish Date | 2016-09-21 | 
| 10610075971647 | Closed System Intermittent Catheter Kit, 16 Fr 16 in, Coude | 
| 10610075971449 | Closed System Intermittent Catheter Kit, 14 Fr 16 in, Coude | 
| 10610075971241 | Closed System Intermittent Catheter Kit, 12 Fr 16 in, Coude | 
| 10610075102140 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Kit, 18 Fr | 
| 10610075102133 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Kit, 16 Fr | 
| 10610075102126 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Kit, 14 Fr | 
| 10610075102119 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Kit, 12 Fr | 
| 10610075102102 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Kit, 10 Fr | 
| 10610075102096 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Kit, 8 Fr | 
| 10610075102089 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Kit, 6 Fr | 
| 10610075102041 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Coude, 16 | 
| 10610075102034 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Coude, 14 | 
| 10610075102027 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, Coude, 12 | 
| 10610075102010 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, 18 Fr 16 i | 
| 10610075101990 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, 16 Fr 16 i | 
| 10610075101983 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, 14 Fr 16 i | 
| 10610075101976 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, 12 Fr 16 i | 
| 10610075101969 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, 10 Fr 16 i | 
| 10610075101952 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, 8 Fr 16 in | 
| 10610075101945 | Pre-lubricated Closed System Intermittent Catheter with Protective Tip and Urine Bag, 6 Fr 16 i | 
| 30610075971443 | Closed System Intermittent Catheter Kit, 14 Fr 16 in, Coude | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  ADVANCE PLUS  90375110  not registered Live/Pending | Cooper Tire & Rubber Company 2020-12-11 | 
|  ADVANCE PLUS  88235605  not registered Live/Pending | SOUTHERN ANESTHESIA & SURGICAL, INC. 2018-12-19 | 
|  ADVANCE PLUS  85548646  4416753 Live/Registered | Mitsubishi Electric Corporation 2012-02-21 | 
|  ADVANCE PLUS  78211809  not registered Dead/Abandoned | Horizon National Bank 2003-02-06 | 
|  ADVANCE PLUS  77672921  3676184 Live/Registered | Hollister Incorporated 2009-02-18 | 
|  ADVANCE PLUS  75023952  not registered Dead/Abandoned | THE DIAL CORP 1995-11-27 |