| Primary Device ID | 00036000411188 | 
| NIH Device Record Key | 81d3c558-c8d3-49d7-9f1f-502f7ffeade1 | 
| Commercial Distribution Discontinuation | 2019-04-04 | 
| Commercial Distribution Status | Not in Commercial Distribution | 
| Brand Name | Poise | 
| Version Model Number | Pessary | 
| Company DUNS | 829568273 | 
| Company Name | KIMBERLY-CLARK GLOBAL SALES, INC. | 
| Device Count | 10 | 
| 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 | true | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | false | 
| OTC Over-The-Counter | true | 
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | |
| Phone | +1(800)340-3102 | 
| xxx@xxx.xxx | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Width | 50 Millimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00036000411188 [Primary] | 
| GS1 | 00036000998467 [Unit of Use] | 
| GS1 | 10036000411185 [Package] Package: Case [4 Units] Discontinued: 2019-04-04 Not in Commercial Distribution | 
| HHW | PESSARY, VAGINAL | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 4 | 
| Public Version Date | 2019-04-04 | 
| Device Publish Date | 2017-03-14 | 
| 00036000411188 | POISE IMPRESSA SIZE 2 BLADDER SUPPORT DEVICE | 
| 00036000411171 | POISE IMPRESSA SIZE 3 BLADDER SUPPORT DEVICE | 
| 10036000411130 | POISE IMPRESSA SIZE 1 BLADDER SUPPORT DEVICE | 
| 00036000496239 | POISE IMPRESSA SIZE 1 BLADDER SUPPORT DEVICE | 
| 00036000496222 | POISE IMPRESSA SIZE 2 BLADDER SUPPORT DEVICE | 
| 00036000496215 | POISE IMPRESSA SIZE 3 BLADDER SUPPORT DEVICE | 
| 00036000496208 | POISE IMPRESSA SIZE 3 BLADDER SUPPORT DEVICE | 
| 00036000496192 | POISE IMPRESSA SIZE 2 BLADDER SUPPORT DEVICE | 
| 00036000496185 | POISE IMPRESSA SIZE 1 BLADDER SUPPORT DEVICE | 
| 00036000470611 | POISE IMPRESSA SIZE 3 BLADDER SUPPORT DEVICE | 
| 00036000470604 | POISE IMPRESSA SIZE 2 BLADDER SUPPORT DEVICE | 
| 00036000470598 | POISE IMPRESSA SIZE 1 BLADDER SUPPORT DEVICE | 
| 10036000465607 | POISE IMPRESSA SIZE 3 BLADDER SUPPORT DEVICE | 
| 10036000465591 | POISE IMPRESSA SIZE 2 BLADDER SUPPORT DEVICE | 
| 10036000465584 | POISE IMPRESSA SIZE 1 BLADDER SUPPORT DEVICE | 
| 00036000431933 | POISE IMPRESSA SIZE 3 BLADDER SUPPORT DEVICE | 
| 00036000431926 | POISE IMPRESSA SIZE 2 BLADDER SUPPORT DEVICE | 
| 00036000431919 | POISE IMPRESSA SIZE 1 BLADDER SUPPORT DEVICE | 
| 10036000411161 | POISE IMPRESSA BLADDER SUPPORT DEVICE | 
| 00036000471335 | POISE IMPRESSA MIXED BLADDER SUPPORT DEVICE 2.541-CASE DISPLAY 13-PKGS | 
| 00036000471328 | POISE IMPRESSA MIXED BLADDER SUPPORT DEVICE 2.5-CASE DISPLAY 10-PACKAGES | 
| 00036000470963 | POISE IMPRESSA MIXED BLADDER SUPPORT DEVICE 2-CASE DISPLAY 8-PACKAGES | 
| 00036000462111 | POISE IMPRESSA BLADDER SUPPORT DEVICE MIXED 3-CS DISPLAY 12-PKG | 
| 00036000462074 | POISE IMPRESSA BLADDER SUPPORT DEVICE MIXED 4-CS DIS 16 PKG | 
| 00036000411164 | POISE IMPRESSA BLADDER SUPPORT DEVICE | 
| 00036000536829 | ONE BY POISE SUPRPREM ULTRATHN REGWNG PAD E-COMM 66 | 
| 00036000536836 | ONE BY POISE SUPRPREM XCVRG FLAT LINER E-COMM 150 | 
| 10036000534501 | ONE BY POISE SUPRPREM ULTRATHN HVYWNG PAD 18 | 
| 10036000534495 | ONE BY POISE SUPRPREM ULTRATHN REGWNG PAD 22 | 
| 10036000534488 | ONE BY POISE SUPRPREM XCVRG FLAT LINER 50 | 
| 00036000670011 | Sample pack containing one of each: 1) One by Poise Extra Coverage Liner,2) One by Poise Heavy P | 
| 00036000541953 | ONE BY POISE SUPRPREM ULTRATHN HVYWNG PAD MIX DSP | 
| 00036000541786 | ONE BY POISE PAD MIX DSP | 
| 00036000597219 | Sample pack contains 2 liners of: One by Poise Extra Coverage Liners, 1 Cottonelle Flushable Wip | 
| 00036000670035 | Sample pack contains one of each: 1) One by Poise Extra Coverage Liner (53451-00),2) One by Pois | 
| 10036000491378 | POISE IMPRESSA SIZING KIT BLADDER SUPPORT DEVICE 3 | 
| 10036000470625 | POISE IMPRESSA SIZING KIT BLADDER SUPPORT DEVICE 6 | 
| 10036000470618 | POISE IMPRESSA SIZE 3 BLADDER SUPPORT DEVICE | 
| 10036000470601 | POISE IMPRESSA SIZE 2 BLADDER SUPPORT DEVICE | 
| 10036000470595 | POISE IMPRESSA SIZE 1 BLADDER SUPPORT DEVICE | 
| 10036000465690 | POISE IMPRESSA BLADDER SUPPORT DEVICE | 
| 00036000491371 | POISE IMPRESSA SIZING KIT BLADDER SUPPORT DEVICE 3 | 
| 00036000475753 | POISE IMPRESSA MIXED BLADDER SUPPORT DEVICE 1-CASE DISPLAY 4-PACKAGES | 
| 00036000470628 | POISE IMPRESSA SIZING KIT BLADDER SUPPORT DEVICE 6 | 
| 00036000465693 | POISE IMPRESSA BLADDER SUPPORT DEVICE | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  POISE  98054536  not registered Live/Pending | Kimberly-Clark Worldwide, Inc. 2023-06-22 | 
|  POISE  88368996  not registered Live/Pending | Johnson & Johnson 2019-04-03 | 
|  POISE  87722712  5519286 Live/Registered | Fantastic Industries, Inc. 2017-12-15 | 
|  POISE  87573409  not registered Dead/Abandoned | Helena Holding Company 2017-08-17 | 
|  POISE  87119143  not registered Dead/Abandoned | ROYAL WINE CORPORATION 2016-07-28 | 
|  POISE  86827394  5094014 Live/Registered | Marquis, David C. 2015-11-20 | 
|  POISE  86315135  not registered Dead/Abandoned | Marquis, David C. 2014-06-19 | 
|  POISE  86236719  4613915 Live/Registered | KIMBERLY-CLARK WORLDWIDE, INC. 2014-03-31 | 
|  POISE  85956587  4637975 Live/Registered | Kimberly-Clark Worldwide, Inc. 2013-06-11 | 
|  POISE  85709054  4280015 Dead/Cancelled | KIMBERLY-CLARK WORLDWIDE, INC. 2012-08-21 | 
|  POISE  85688416  4279971 Dead/Cancelled | KIMBERLY-CLARK WORLDWIDE, INC. 2012-07-27 | 
|  POISE  85651288  not registered Dead/Abandoned | Poison LLC 2012-06-13 |