| Primary Device ID | 00810170013744 |
| NIH Device Record Key | 4686ec86-13a9-4d79-a1ae-e592bf111294 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Headway Advanced Soft |
| Version Model Number | MC172150S |
| Catalog Number | MC172150S |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810170013744 [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 | 2020-01-14 |
| Device Publish Date | 2016-09-24 |
| 00842429108444 - Sofia | 2024-10-28 Sofia 6F-115cm STR |
| 00842429108451 - Sofia | 2024-10-28 Sofia 6F-125cm STR |
| 00842429108468 - Sofia | 2024-10-28 Sofia 6F-131cm STR |
| 00842429108475 - Sofia | 2024-10-28 Sofia 6F-125cm STR |
| 00842429118092 - Access | 2024-10-28 Sofia EX 5F - 115cm STR |
| 00842429119396 - Wedge | 2024-10-28 Wedge XL |
| 00842429108482 - Sofia | 2024-08-14 Sofia 6F-131cm STR |
| 00842429117705 - SOFIA 88 | 2023-06-23 SOFIA 88 - 115cm |