Primary Device ID | 20817470009761 |
NIH Device Record Key | a961e15a-ba9b-4a78-a69a-4e981a5fe0cd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ENT Sinus |
Version Model Number | 602-00210 |
Catalog Number | 602-00210 |
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 | 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)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 | |
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 | 00817470009767 [Primary] |
GS1 | 20817470009761 [Package] Contains: 00817470009767 Package: BX [4 Units] In Commercial Distribution |
LYA | SPLINT, INTRANASAL SEPTAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-01-31 |
Device Publish Date | 2015-08-30 |
00817470011869 | SERPENT STERILIZATION TRAY LID |
00817470011845 | SERPENT STERILIZATION TRAY BASE |
20817470009761 | MEDIENT MIDDLE TURBINATE IMPLANT 4-PACK |
00817470009750 | MediENT Middle Turbinate Implant 1-pack |
00817470009729 | VENTERA SINUS DILATION BALLOON 1-PACK |
00817470006469 | ENTACT SEPTAL STAPLER 1-PACK |
20817470006456 | ENTACT SEPTAL STAPLER 3-PACK |
00885556724736 | SERPENT STERILIZATION TRAY LID |