Q-FIX 72290033
GUDID 00885556630792
REUSABLE 1.8MMQ-FIX OBTURATOR
Smith & Nephew, Inc.
Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator Surgical drill guide obturator| Primary Device ID | 00885556630792 |
| NIH Device Record Key | 9b940429-52e1-4278-b51e-fe3f2c8016ae |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Q-FIX |
| Version Model Number | 72290033 |
| Catalog Number | 72290033 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| 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 | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885556630792 [Primary] |
FDA Product Code
| NBH | Accessories, arthroscopic |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
[00885556630792]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-04-13 |
| Device Publish Date | 2023-04-05 |
On-Brand Devices [Q-FIX]
| 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 |
Trademark Results [Q-FIX]
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 |
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