Invuity® Fiber Optic Sterilization Tray 110210
GUDID 00816728020271
The Invuity® Fiber Optic Sterilization Tray is intended to allow sterilization of the enclosed medical devices.
INVUITY, INC.
Sterilization/disinfection container Sterilization/disinfection container Sterilization/disinfection container Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable| Primary Device ID | 00816728020271 |
| NIH Device Record Key | 47a1a1e9-160b-46ae-84e5-bf237520a09d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Invuity® Fiber Optic Sterilization Tray |
| Version Model Number | Large |
| Catalog Number | 110210 |
| Company DUNS | 175697908 |
| Company Name | INVUITY, 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Height | 1.5 Inch |
| Height | 1.5 Inch |
| Height | 1.5 Inch |
| Height | 1.5 Inch |
| Height | 1.5 Inch |
| Height | 1.5 Inch |
| Height | 1.5 Inch |
| Height | 1.5 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
| Width | 15 Inch |
| Depth | 10 Inch |
| Height | 1.5 Inch |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816728020271 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K090070
FDA Product Code
| FST | Light, Surgical, Fiberoptic |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
[00816728020271]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2020-04-24 |
| Device Publish Date | 2016-09-22 |
Devices Manufactured by INVUITY, INC.
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| 00816728021582 - Eikon LT Adapt Smoke Evacuation | 2020-04-24 Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the devic |
| 00816728021124 - Eikon LT Adapt Smoke Evacuation | 2020-04-24 Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the devic |
| 00816728021131 - Eikon LT Adapt Smoke Evacuation | 2020-04-24 Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the devic |
| 00816728021599 - Eikon LT Adapt Smoke Evacuation | 2020-04-24 Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the devic |
| 00816728021605 - Eikon LT Adapt Smoke Evacuation | 2020-04-24 Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the devic |
| 00816728021162 - Eikon LT Adapt Smoke Evacuation | 2020-04-24 Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the devic |
Trademark Results [Invuity]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INVUITY 77976634 3604233 Live/Registered |
INVUITY, INC. 2007-09-28 |
 INVUITY 77292075 not registered Dead/Abandoned |
INVUITY, INC. 2007-09-28 |
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