| Primary Device ID | 00812636020945 | 
| NIH Device Record Key | 15d0bb49-74a4-4272-a67f-88c599552b31 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Headway | 
| Version Model Number | MC212156S | 
| Catalog Number | MC212156S | 
| Company DUNS | 003263105 | 
| Company Name | MICROVENTION INC. | 
| Device Count | 1 | 
| DM Exempt | true | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Conditional | 
| 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 | true | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| 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 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 | 00812636020945 [Primary] | 
| DQY | CATHETER, PERCUTANEOUS | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 5 | 
| Public Version Date | 2020-01-13 | 
| Device Publish Date | 2016-09-24 | 
| 00811425021385 | Microcatheter | 
| 00811425020449 | Microcatheter | 
| 00810170016165 | Microcatheter | 
| 00810170014857 | Microcatheter | 
| 00812636020945 | Microcatheter | 
| 04987350609199 | Microcatheter | 
| 00842429117507 | Headway | 
| 00842429117484 | Headway | 
| 00842429117460 | Headway Advanced | 
| 00842429117453 | Headway Advanced | 
| 00842429117446 | Headway Advanced | 
| 00842429117439 | Headway Advanced | 
| 00842429117422 | Headway Advanced Soft | 
| 00842429117415 | Headway Duo | 
| 00842429117408 | Headway Duo |