Primary Device ID | 10886874117306 |
NIH Device Record Key | c2647602-32e9-403a-bc7a-d906f78b4521 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | da Vinci Energy |
Version Model Number | 480440 |
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 | 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 |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Outer Diameter | 8 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886874117309 [Primary] |
GS1 | 10886874117306 [Package] Contains: 00886874117309 Package: BOX [6 Units] In Commercial Distribution |
NAY | System, surgical, computer controlled instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-03-02 |
Device Publish Date | 2019-12-10 |
10886874117306 | SynchroSeal |
00886874116982 | E-100 Generator |
00886874123867 | E-200 Gen 4 Generator Upgrade |
00886874120880 | E-200 Generator |
00886874124000 | Da Vinci Monopolar and Bipolar Adapters |