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 |