| Primary Device ID | 00607567700451 |
| NIH Device Record Key | 8cbebde3-a872-4e1a-836a-7ebab678c0e6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hemopro 2 w/Vasoshield |
| Version Model Number | VH-4001 |
| Catalog Number | VH-4001 |
| Company DUNS | 022348156 |
| Company Name | MAQUET CARDIOVASCULAR LLC |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| 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 | 888-880-2874 |
| cssurgery@maquet.com | |
| Phone | 888-880-2874 |
| cssurgery@maquet.com | |
| Phone | 888-880-2874 |
| cssurgery@maquet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00607567700451 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
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