Primary Device ID | 00810275013021 |
NIH Device Record Key | 0df76129-3eda-4ee3-8d16-81c372880ad6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 7.5mm Cartridge |
Version Model Number | R2175 |
Company DUNS | 143602659 |
Company Name | ENDOGASTRIC SOLUTIONS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | 425-307-9269 |
customerservice@endogastricsolutions.com | |
Phone | 425-307-9269 |
customerservice@endogastricsolutions.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810275013021 [Primary] |
ODE | Endoscopic Suture/Plication System, Gastroesophageal Reflux Disease (Gerd) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
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