Primary Device ID | 00886874110164 |
NIH Device Record Key | 260b7b68-b7d2-45bf-b395-771107e0ca52 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ikegami |
Version Model Number | 370884 |
Company DUNS | 938647021 |
Company Name | INTUITIVE SURGICAL, 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 |
Length | 43 Feet |
Length | 43 Feet |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886874110164 [Primary] |
NAY | System,surgical,computer controlled instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-03-02 |
Device Publish Date | 2016-07-08 |
00886874123997 - daVinci 5 | 2024-04-03 BLUE SYSTEM CABLE |
00886874124017 - daVinci 5 | 2024-04-03 CO2 Supply Tank Interface Device |
10886874120696 - None | 2024-04-02 TUBE SET WITH SMOKE EVACUATION |
00886874120286 - None | 2024-04-01 ENDOSCOPE |
00886874120293 - None | 2024-04-01 ENDOSCOPE |
00886874122099 - None | 2024-04-01 8MM HEX CANNULA, LONG |
00886874122105 - None | 2024-04-01 8MM HEX CANNULA, STANDARD |
00886874119662 - daVinci 5 | 2024-03-29 Vision Side Cart |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
IKEGAMI 74622997 1942763 Live/Registered |
Ikegami Tsushinki Co., Ltd. 1995-01-19 |
IKEGAMI 74081508 1658845 Dead/Cancelled |
IKEGAMI TSUSHINKI CO., LTD. 1990-07-24 |
IKEGAMI 73217457 1165312 Live/Registered |
Ikegami Tsushinki Co., Ltd. 1979-05-29 |