| Primary Device ID | 00842071144975 |
| NIH Device Record Key | 8df800f2-1b3f-4b6a-acba-b9a56ccbf769 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GEMINI |
| Version Model Number | ESD221S-07 |
| Catalog Number | ESD221S-07, SD221S-07-101, SD221S-07-105 |
| Company DUNS | 038101861 |
| Company Name | APPLIED MEDICAL TECHNOLOGY, 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 | true |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net | |
| Phone | (440)717-4000 |
| cs@appliedmedical.net |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842071144968 [Primary] |
| GS1 | 00842071144975 [Package] Contains: 00842071144968 Package: Box (SD221S-07-101) [1 Units] In Commercial Distribution |
| GS1 | 00842071144982 [Package] Contains: 00842071144968 Package: Box (SD221S-07-105) [5 Units] In Commercial Distribution |
| GCJ | Laparoscope, General & Plastic Surgery |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-10-14 |
| Device Publish Date | 2024-10-04 |
| 00842071145002 | GEMINI Suture Passer with Magnet Technology (Curved Needle, Pouched) |
| 00842071144975 | GEMINI Suture Passer with Magnet Technology (Straight Needle, Pouched) |
| 00842071149017 | GEMINI Suture Passer with Magnet Technology (Curved Needle, Pouched) |
| 00842071148980 | GEMINI Suture Passer with Magnet Technology (Straight Needle, Pouched) |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GEMINI 98873161 not registered Live/Pending |
Grant Prideco, Inc. 2024-11-26 |
![]() GEMINI 98656156 not registered Live/Pending |
Applied Medical Technology, Inc. 2024-07-18 |
![]() GEMINI 98585431 not registered Live/Pending |
Cooper Machinery Services LLC 2024-06-05 |
![]() GEMINI 98567891 not registered Live/Pending |
WONIK IPS CO., LTD. 2024-05-24 |
![]() GEMINI 98484508 not registered Live/Pending |
Ballyhoo Hospitality, LLC 2024-04-04 |
![]() GEMINI 98484468 not registered Live/Pending |
Ballyhoo Hospitality, LLC 2024-04-04 |
![]() GEMINI 98425860 not registered Live/Pending |
Sunseeker U.S. Inc. 2024-02-28 |
![]() GEMINI 98418146 not registered Live/Pending |
Google LLC 2024-02-23 |
![]() GEMINI 98202646 not registered Live/Pending |
Google LLC 2023-09-28 |
![]() GEMINI 98170099 not registered Live/Pending |
Gemini IP, LLC 2023-09-07 |
![]() GEMINI 97772796 not registered Live/Pending |
AMC Performance Textiles, LLC 2023-01-30 |
![]() GEMINI 97648185 not registered Live/Pending |
DIRECTV, LLC 2022-10-26 |