| Primary Device ID | 00885556724781 |
| NIH Device Record Key | 2ab417a0-0b6b-4641-9df7-7bc7c46d60d9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ACCU-PASS |
| Version Model Number | OM-9892 |
| Catalog Number | OM-9892 |
| Company DUNS | 109903521 |
| Company Name | Smith & Nephew, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885556724781 [Primary] |
| HWQ | PASSER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-02-06 |
| Device Publish Date | 2018-07-12 |
| 00817470012200 | ACCU-PASS DIRECT CRESCENT XL |
| 00885556724798 | ACCU-PASS DIRECT; 90 DEG UP |
| 00885556724781 | ACCU-PASS DIRECT; 45 DEG RIGHT |
| 00885556724774 | ACCU-PASS DIRECT; 45 DEG LEFT |
| 00885556724767 | ACCU-PASS DIRECT; CRESCENT |
| 00885556724569 | ACCU-PASS DIRECT CRESCENT XL |
| 23596010596370 | ACCU-PASS SUT SHUTTLE MONOFILAMENT 1 |
| 23596010576075 | ACCUPASS STR SHUTL MONOFIL -SEE72201361 |
| 03596010543349 | ACCU-PASS STR SHTL BIG C STERILE BOX 1 |
| 03596010542397 | ACCU-PASS SUTURE SHUTTLE 70 DEGREE |
| 03596010534484 | ACCU-PASS STR SHUTTLE CRESCENT |
| 03596010534477 | ACCU-PASS STR SHUTTLE STRAIGHT |
| 03596010534460 | ACCU-PASS STR SHUTTLE 45 DEG UP |
| 03596010534453 | ACCU-PASS STR SHUTTLE 45 DEG RGHT CRVE |
| 03596010534446 | ACCU-PASS STR SHUTTLE 45 DEG LFT CURVE |
| 03596010601391 | ACCU-PASS SUTURE SHUTTLE J-HOOK STERIL |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACCU-PASS 78560667 3146779 Live/Registered |
Smith & Nephew, Inc. 2005-02-04 |
![]() ACCU-PASS 76100748 not registered Dead/Abandoned |
Orthopaedic Biosystems Ltd., Inc. 2000-08-01 |