EntreVu EVEX-8-7T
GUDID 20866497000329
Instrument Cannula
Cannuflow, Inc.
Arthroscopic access cannula, single-use| Primary Device ID | 20866497000329 |
| NIH Device Record Key | cabc9bd2-1bc4-4323-98af-d2b8111c6526 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EntreVu |
| Version Model Number | EX-8-7T |
| Catalog Number | EVEX-8-7T |
| Company DUNS | 138461384 |
| Company Name | Cannuflow, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 |
Device Dimensions
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00866497000325 [Primary] |
| GS1 | 20866497000329 [Package] Contains: 00866497000325 Package: Shelf Box [5 Units] In Commercial Distribution |
FDA Product Code
| FGY | Cannula, Injection |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
[20866497000329]
Radiation Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-24 |
| Device Publish Date | 2024-01-16 |
Devices Manufactured by Cannuflow, Inc.
| 20860002896933 - SportPort | 2024-01-24 Flexible Access Portal Kit |
| 20860002896940 - SportPort | 2024-01-24 Flexible Access Port Kit |
| 20866497000305 - ClearVu 2.7 Blunt | 2024-01-24 Flexible Inflow-Outflow Cannula |
| 20866497000312 - ClearVu 2.7 Sharp | 2024-01-24 Flexible Inflow-Outflow Cannula |
| 20866497000329 - EntreVu | 2024-01-24Instrument Cannula |
| 20866497000329 - EntreVu | 2024-01-24 Instrument Cannula |
| 20866497000336 - ExtravaStopper | 2024-01-24 Portal Plug |
| 20866497000343 - TwoVu | 2024-01-24 Outflow Sheath |
| 20866497000350 - TwoVu | 2024-01-24 Outflow Sheath |
Trademark Results [EntreVu]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ENTREVU 77009766 3278471 Live/Registered |
Cannuflow, Inc. 2006-09-28 |
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