Primary Device ID | 00817470011845 |
NIH Device Record Key | 0633be31-bc32-41e8-8b91-4a553af2a413 |
Commercial Distribution Discontinuation | 2018-08-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ENT Sinus |
Version Model Number | 910-30105 |
Catalog Number | 910-30105 |
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 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00817470011845 [Primary] |
MMO | TRAY, SURGICAL, ENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00817470011845]
Moist Heat or Steam Sterilization
[00817470011845]
Moist Heat or Steam Sterilization
[00817470011845]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-08-09 |
Device Publish Date | 2015-08-29 |
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 |