| Primary Device ID | 20866497000367 |
| NIH Device Record Key | e0919101-c6a6-4085-a5b5-deddd92a56ce |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TwoVu |
| Version Model Number | ST-6L |
| Catalog Number | TVST-6L |
| 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 |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Outer Diameter | 5.8 Millimeter |
| Length | 123 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00866497000363 [Primary] |
| GS1 | 20866497000367 [Package] Contains: 00866497000363 Package: Shelf Box [5 Units] In Commercial Distribution |
| FGY | Cannula, Injection |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
[20866497000367]
Radiation Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-24 |
| Device Publish Date | 2024-01-16 |
| 20866497000374 | Outflow Sheath |
| 20866497000367 | Outflow Sheath |
| 20866497000350 | Outflow Sheath |
| 20866497000343 | Outflow Sheath |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TWOVU 77009748 3267522 Live/Registered |
Cannuflow, Inc. 2006-09-28 |