Suturefix E0015073-1
GUDID 00885556653364
MODIFIED SUTUREFIX GUIDE
Smith & Nephew, Inc.
Surgical drill guide, reusable| Primary Device ID | 00885556653364 |
| NIH Device Record Key | 839153f5-a41f-40b1-82f7-455ddfe6954e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Suturefix |
| Version Model Number | E0015073-1 |
| Catalog Number | E0015073-1 |
| Company DUNS | 109903521 |
| Company Name | Smith & Nephew, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885556653364 [Primary] |
FDA Product Code
| MBI | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
[00885556653364]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-11-22 |
| Device Publish Date | 2016-06-29 |
On-Brand Devices [Suturefix]
| 00885556737262 | CURVED SUTUREFIX GUIDE |
| 00885556668306 | SUTUREFIX GUIDE WITH MODIFIED TIP |
| 00885556660133 | SUTUREFIX GUIDE WITH MODIFIED TIP |
| 00885556653364 | MODIFIED SUTUREFIX GUIDE |
| 00885556706466 | SUTUREFIX GD FR ULTRA STRT DEV XL LNGTH |
| 00885556706459 | SUTUREFIX GUIDE ULTRA STRT DEV S LNGTH |
Trademark Results [Suturefix]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SUTUREFIX 88214858 not registered Live/Pending |
Smith & Nephew, Inc. 2018-12-03 |
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