| Primary Device ID | 00842429118733 | 
| NIH Device Record Key | 5810fd87-b6d6-433d-a921-c1778633ec16 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | VIA Microcatheter | 
| Version Model Number | VIA-33-133-01-AL | 
| Catalog Number | VIA-33-133-01 | 
| Company DUNS | 003263105 | 
| Company Name | MICROVENTION INC. | 
| Device Count | 1 | 
| DM Exempt | true | 
| 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 | true | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | true | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | |
| Phone | +1(714) 247-8000 | 
| customerservice@microvention.com | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00842429118733 [Primary] | 
| KRA | Catheter, continuous flush | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2025-05-08 | 
| Device Publish Date | 2025-04-30 | 
| 00842429106457 | VIA 17 Microcatheter | 
| 00842429106440 | VIA 17 Microcatheter | 
| 00842429106433 | VIA 33 Microcatheter | 
| 00842429106426 | VIA 27 Microcatheter | 
| 00842429106419 | VIA 21 Microcatheter | 
| 00842429106402 | VIA 17 Microcatheter | 
| 00842429118757 | VIA 17 Microcatheter | 
| 00842429118740 | VIA 17 Microcatheter | 
| 00842429118733 | VIA 33 Microcatheter | 
| 00842429118726 | VIA 27 Microcatheter | 
| 00842429118702 | VIA 17 Microcatheter |