| Primary Device ID | 00817081020076 |
| NIH Device Record Key | 800fd053-3c73-4409-abd6-0c727886c90e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VBMax |
| Version Model Number | VBMax30S - 136300 |
| Catalog Number | 136300 |
| Company DUNS | 020275145 |
| Company Name | A-M SYSTEMS, 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817081020045 [Primary] |
| GS1 | 00817081020076 [Package] Contains: 00817081020045 Package: Individually Bagged [50 Units] In Commercial Distribution |
| GS1 | 00817081021387 [Package] Contains: 00817081020045 Package: [100 Units] In Commercial Distribution |
| CAH | Filter, Bacterial, Breathing-Circuit |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-08-14 |
| Device Publish Date | 2016-09-24 |
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| 00817081020137 | VBMax31S Disposable PF Testing Filter |
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