Primary Device ID | 10893029002240 |
NIH Device Record Key | 013abb7b-ff86-4991-b10a-9084a815e142 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EverLift |
Version Model Number | GIS-59 |
Catalog Number | GIS-59 |
Company DUNS | 160990313 |
Company Name | GI Supply, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00893029002243 [Primary] |
GS1 | 10893029002240 [Package] Contains: 00893029002243 Package: [10 Units] In Commercial Distribution |
PLL | Submucosal Injection Agent |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-02-26 |
Device Publish Date | 2021-02-18 |
10893029002240 | Submucosal Lifting Agent - 10mL Single Unit |
00893029002229 | Submucosal Lifting Agent - 5mL Single Unit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EVERLIFT 98191080 not registered Live/Pending |
Cybership, Inc 2023-09-21 |
EVERLIFT 98174749 not registered Live/Pending |
Cybership, Inc 2023-09-11 |
EVERLIFT 88171369 not registered Live/Pending |
GI Supply, Inc. 2018-10-26 |
EVERLIFT 87632741 5531855 Live/Registered |
Piasecki, Justin H., M.D. 2017-10-04 |
EVERLIFT 87611210 not registered Dead/Abandoned |
Digital Phoenix, LLC 2017-09-16 |