Primary Device ID | 00840253109521 |
NIH Device Record Key | e12ad536-c9f0-4d27-949c-1e04bbd49d68 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fuse® |
Version Model Number | FDEMO-F7523 |
Company DUNS | 014154279 |
Company Name | ENDOCHOICE, 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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com | |
Phone | 888-632-3636 |
customercare@endochoice.com |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Length | 168 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840253109521 [Primary] |
FDF | Colonoscope And Accessories, Flexible/Rigid |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-06-21 |
Device Publish Date | 2016-09-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FUSE 98650787 not registered Live/Pending |
Nexgrill Industries, Inc. 2024-07-16 |
FUSE 98576075 not registered Live/Pending |
Sig Sauer Inc. 2024-05-30 |
FUSE 98463826 not registered Live/Pending |
Sandata Technologies, LLC 2024-03-22 |
FUSE 98366092 not registered Live/Pending |
Fuse Diagnostics Limited 2024-01-19 |
FUSE 98292817 not registered Live/Pending |
HDA Truck Pride, Inc. 2023-11-30 |
FUSE 98196482 not registered Live/Pending |
FUSE APP CORP 2023-09-25 |
FUSE 98092258 not registered Live/Pending |
Tesseract Laboratories Limited 2023-07-19 |
FUSE 97760566 not registered Live/Pending |
Trauman, Todd 2023-01-19 |
FUSE 97620026 not registered Live/Pending |
Trauman, Todd 2022-10-05 |
FUSE 97589516 not registered Live/Pending |
FUSE, LLC 2022-09-13 |
FUSE 97576992 not registered Live/Pending |
Lashify, Inc. 2022-09-02 |
FUSE 97524293 not registered Live/Pending |
Master Tailgaters, LLC 2022-07-28 |