Primary Device ID | 00885556630761 |
NIH Device Record Key | 0af55162-5c9c-4b36-b3cb-09b665a03057 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Q-FIX |
Version Model Number | 72290030 |
Catalog Number | 72290030 |
Company DUNS | 045483575 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00885556630761 [Primary] |
LXH | Orthopedic manual surgical instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-14 |
Device Publish Date | 2024-05-06 |
00885556724644 | 2.8MM Q-FIX ALL SUTURE ANCHOR |
00885556724606 | 1.8MM Q-FIX ALL SUTURE ANCHOR |
00885556657461 | 1.8MM QFIX REUSABLE CURVED DRILLGUIDE 24 |
00885556657454 | 1.8MM QFIX RESUABLE CURVED DRILLGUIDE 12 |
00885556657447 | 1.8MM Q-FIX DISPOSABLE FLEXIBLE DRILL |
00885556630815 | REUSABLE 2.8MM Q-FIX DRILL GUIDE |
00885556662618 | QFIX 1.8 MINI SUTURE ANCHOR |
00885556630792 | REUSABLE 1.8MMQ-FIX OBTURATOR |
00885556885406 | 2.8MM Q-FIX ALL-SUTURE ANCHOR WITH TWO MINITAPE SUTURES (BLU |
00885556885390 | 1.8MM Q-FIX ALL-SUTURE ANCHOR WITH ONE MINITAPE SUTURE (BLUE |
00885556885383 | 1.8MM Q-FIX ALL-SUTURE ANCHOR WITH ONE MINITAPE SUTURE (COBR |
00885556885642 | Q-FIX WITH NEEDLES - MINITAPE |
00885556885635 | Q-FIX WITH NEEDLES #0 SUTURE |
00885556885598 | DRILL FOR Q-FIX WITH NEEDLES |
00885556890790 | 2.9MM CANNULATED DRILL FOR Q-FIX ULTRA & 1.25MM DRILL PIN |
00885556890745 | Q-FIX ULTRA |
00885556630785 | REUSABLE 1.8MMQ-FIX DRILL GUIDE |
00885556630761 | DISPOSABLE 1.8MM Q-FIX DRILL |
00885556901687 | Q-FIX KNOTLESS ALL-SUTURE ANCHOR 1.8MM WITH ONE ULTRABRAID SUTURE BLUE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
Q-FIX 98060364 not registered Live/Pending |
QCI Co., Ltd. 2023-06-27 |
Q-FIX 85892136 4589613 Live/Registered |
ArthroCare Corporation 2013-04-01 |