Primary Device ID | 10845854026304 |
NIH Device Record Key | 2294dd8e-77e4-49b9-b41c-f8b49ffe4fcc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SHUTT |
Version Model Number | 9896 |
Catalog Number | 9896 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854026304 [Primary] |
GS1 | 20845854026301 [Direct Marking] |
FSM | TRAY, SURGICAL, INSTRUMENT |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2020-04-28 |
10845854026304 | Shutt Small Joint Arthroscopy Instrument Case |
30845854026322 | SHUTT ARTHROSCOPY INSTRUMENT CASE |
30845854026216 | SHUTT MASTER SET STERILIZATION CASE, METAL |
20845854026325 | SHUTT ARTHROSCOPY INSTRUMENT CASE |
20845854026219 | SHUTT MASTER SET STERILIZATION CASE, METAL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SHUTT 88132905 not registered Live/Pending |
Shutt Automotive, Inc. 2018-09-26 |
SHUTT 77139986 3866011 Dead/Cancelled |
Ueni Industria Comercia Importacao e Exportacao Ltda. 2007-03-26 |
SHUTT 73716477 1557793 Live/Registered |
CONCEPT, INC. 1988-03-14 |