| Primary Device ID | 00840253111067 |
| NIH Device Record Key | e4fd47cc-73a7-44c7-92cf-d45fcdbbdddd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fuse® |
| Version Model Number | LS-FSC330-F7524 |
| 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 | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Length | 133 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840253111067 [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 |