Force Feedback
GUDID 10886874120733
Force Feedback Maryland Bipolar Forceps
INTUITIVE SURGICAL, INC.
Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable Robotic electrosurgical instrument, bipolar, reusable| Primary Device ID | 10886874120733 |
| NIH Device Record Key | 6b7d41d3-9398-4c2b-8b2b-3dfbc06148ad |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Force Feedback |
| Version Model Number | 475172 |
| 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 | true |
| Serial Number | false |
| 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 |
Device Dimensions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886874120736 [Primary] |
| GS1 | 10886874120733 [Package] Contains: 00886874120736 Package: BOX [5 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K232610
FDA Product Code
| NAY | System, surgical, computer controlled instrument |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
[10886874120733]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-29 |
| Device Publish Date | 2024-03-21 |
On-Brand Devices [Force Feedback]
| 10886874120757 | Force Feedback Mega SutureCut Needle Driver |
| 10886874120740 | Force Feedback Fenestrated Bipolar Forceps |
| 10886874120733 | Force Feedback Maryland Bipolar Forceps |
| 10886874120726 | Force Feedback ProGrasp Forceps |
| 10886874120719 | Force Feedback Cadiere Forceps |
| 10886874120702 | Force Feedback Large Needle Driver |
Trademark Results [Force Feedback]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FORCE FEEDBACK 75912590 not registered Dead/Abandoned |
Playmates Toys Inc. 2000-02-09 |
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