| Primary Device ID | 00885554031553 |
| NIH Device Record Key | f02f83fa-4396-4e05-b816-56d96d502b58 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ULTRABRAID |
| Version Model Number | 72203842 |
| Catalog Number | 72203842 |
| Company DUNS | 109903521 |
| Company Name | Smith & Nephew, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885554031553 [Primary] |
| MBI | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-01-31 |
| Device Publish Date | 2015-10-05 |
| 20885554034855 | ULTRABRAID 2-0 COBRA 24 W/NEED 10 PACK |
| 20885554034848 | ULTRABRAID 2-0 WHITE 24 W/NEED 10 PACK |
| 00885554031898 | (5) SUTUREFIX AHR S (1) 2 UB BL 1.9 |
| 00885554031881 | (5) SUTUREFIX AHR S (1) 2 UB BL 1.7 |
| 00885554031553 | SUTUREFIX ULTRA AHR XL 2 UB BLUE/WH |
| 00885554031447 | SUTUREFIX ULTRA AHR S 2 UB STR CB BLU |
| 00885554030051 | SUTUREFIX UL ANR XL W/1 2 ULTRABRIAD BL |
| 00885554030044 | SUTUREFIX ULTRA AHR S W/2 UB STR 1 BL |
| 00885554030037 | SUTUREFIX ULTRA AHR S 2 UB STR BLUE |
| 20885554017650 | ULTRABRAID II 2 BLUE SUTURE 38 |
| 03596010587664 | SUTURE 2 CO-BRAID ULTRABRAID 38 |
| 03596010587657 | SUTURE 2 WHITE ULTRABRAID 38 |
| 03596010547682 | ULTRBRD2 COBRAID 38 SNGL ARM PACK AS |
| 03596010547675 | ULTRBRD2 WHT 38SNGL ARM PCK ASSY |
| 23596010511946 | ULTRABRAID 2 WHITE 38 LENGTH SINGLE |
| 23596010511939 | ULTRABRAID 2 COBRAID 38 LENGTH SINGL |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ULTRABRAID 87295567 5399450 Live/Registered |
CONTITECH USA, INC. 2017-01-10 |
![]() ULTRABRAID 78396630 3018683 Live/Registered |
Smith & Nephew, Inc. 2004-04-05 |
![]() ULTRABRAID 74616974 2005137 Dead/Cancelled |
Jim Ray Co., Inc. 1994-12-30 |