| Primary Device ID | 20860002896964 |
| NIH Device Record Key | ab653f0b-8b57-43f9-bb30-f0f9a7bec6a7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Talarus |
| Version Model Number | Talarus 3-3 |
| Catalog Number | TAL 3-3 |
| Company DUNS | 138461384 |
| Company Name | Cannuflow, Inc. |
| Device Count | 1 |
| DM Exempt | true |
| 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 |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Length | 30 Millimeter |
| Lumen/Inner Diameter | 3.8 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860002896960 [Primary] |
| GS1 | 20860002896964 [Package] Contains: 00860002896960 Package: Shelf Box [5 Units] In Commercial Distribution |
| GEA | Cannula, Surgical, General & Plastic Surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
[20860002896964]
Radiation Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-02-05 |
| Device Publish Date | 2026-01-28 |
| 20860002896964 - Talarus | 2026-02-05Small Joint Cannula |
| 20860002896964 - Talarus | 2026-02-05 Small Joint Cannula |
| 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 | 2024-01-24 Instrument Cannula |
| 20866497000336 - ExtravaStopper | 2024-01-24 Portal Plug |
| 20866497000343 - TwoVu | 2024-01-24 Outflow Sheath |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TALARUS 90483398 not registered Live/Pending |
Cannuflow, Inc. 2021-01-22 |
![]() TALARUS 88787825 not registered Live/Pending |
BASF SE 2020-02-06 |