| Primary Device ID | 20816203023272 | 
| NIH Device Record Key | 9802efe5-ab71-4229-b125-bb16431de525 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | PVC Transfer Bag | 
| Version Model Number | 10-200 | 
| Company DUNS | 625272232 | 
| Company Name | ORIGEN BIOMEDICAL, INC. | 
| Device Count | 2 | 
| 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 | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | |
| Phone | 512-474-7278 | 
| regulatory@origen.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00816203023278 [Unit of Use] | 
| GS1 | 10816203023275 [Primary] | 
| GS1 | 20816203023272 [Package] Contains: 10816203023275 Package: Case [24 Units] In Commercial Distribution | 
| KSR | Container, Empty, For Collection & Processing Of Blood & Blood Components | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 4 | 
| Public Version Date | 2021-01-08 | 
| Device Publish Date | 2017-06-06 | 
| 20816203023296 | Two 200ml PVC processing bags, with a male luer, a female luer, a needle-free injection port, a | 
| 20816203023289 | Two 200ml PVC processing bag, with a male luer, a female luer, a needle-free injection port and | 
| 20816203023272 | One 200ml PVC processing bag, with a male luer, a female luer, a needle-free injection port and |