Primary Device ID | 00885556724774 |
NIH Device Record Key | c8d79bfe-281b-47fb-bd68-a6bdb3df28a3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACCU-PASS |
Version Model Number | OM-9891 |
Catalog Number | OM-9891 |
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 | 00885556724774 [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 |