Primary Device ID | 20817470007262 |
NIH Device Record Key | 0749efde-108a-45bf-8d0f-b5d399a66f04 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MAGNUMWIRE |
Version Model Number | OM-9042 |
Catalog Number | OM-9042 |
Company DUNS | 109903521 |
Company Name | Smith & Nephew, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817470007268 [Primary] |
GS1 | 20817470007262 [Package] Contains: 00817470007268 Package: BX [12 Units] In Commercial Distribution |
GAT | SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-31 |
Device Publish Date | 2015-10-08 |
20817470007309 | MAGNUMWIRE BLACK COBRAID SUTURE W NEEDLE |
20817470007293 | LOOSE MAGNUMWIRE SUTURE CO-BRAID WITH 26 |
20817470007286 | LOOSE MAGNUMWIRE SUTURE WHITE WITH 26 MM |
20817470007279 | MAGNUMWIRE SUTURE CO-BRAID |
20817470007262 | MAGNUMWIRE SUTURE BLACK 12 PER BOX |
20817470007255 | MAGNUMWIRE SUTURE WHITE 12 PER BOX |
00817470005936 | MAGNUMWIRE SURGICAL SCISSOR PKG |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MAGNUMWIRE 78289500 3030155 Live/Registered |
ARTHROCARE CORPORATION 2003-08-19 |