ENDO-FIX 7207358D
GUDID 03596010656490
REFURB DRVR.ENDO-FIX L
Smith & Nephew, Inc.
Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable| Primary Device ID | 03596010656490 |
| NIH Device Record Key | 737e7775-f71a-4a2e-904e-c403841a94b6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENDO-FIX |
| Version Model Number | 7207358D |
| Catalog Number | 7207358D |
| 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)821-5700 |
| 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 | 03596010656490 [Primary] |
FDA Product Code
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
[03596010656490]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-01-31 |
| Device Publish Date | 2015-09-28 |
On-Brand Devices [ENDO-FIX]
| 03596010656490 | REFURB DRVR.ENDO-FIX L |
| 03596010411235 | SCR INTER. ENDO-FIX L 8X25MM |
| 03596010411228 | SCR.INTF.ENDOFX 8X20MM |
Trademark Results [ENDO-FIX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ENDO-FIX 74237139 1803688 Dead/Cancelled |
SMITH & NEPHEW, INC. 1992-01-13 |
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