| Primary Device ID | 03596010113702 |
| NIH Device Record Key | 17ed1adc-f9bd-4b9c-b63e-32714c4e024e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GEMINI |
| Version Model Number | 3004 |
| Catalog Number | 3004 |
| Company DUNS | 109903521 |
| Company Name | Smith & Nephew, 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 | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03596010113702 [Primary] |
| GCJ | Laparoscope, general & plastic surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
[03596010113702]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-31 |
| Device Publish Date | 2015-08-30 |
| 00885554008739 | LT GUIDE GEMINI 4MM X 12FT |
| 03596010528933 | GEMINI UNIVERSAL LT GUIDE 4MM |
| 03596010430847 | LIGHT GUIDE 6MM 10FT |
| 03596010251107 | LT. GUIDE GEMINI 5MM X 12FT |
| 03596010113702 | LIGHT CABLE 2MM X 8FT |
| 03596010113634 | GEMINI LIGHT CABLE 4MM X 8 FT |
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 |