| Primary Device ID | 14719878520505 |
| NIH Device Record Key | 8a7ea72a-4e05-451a-9881-bf9ae84eea72 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Puriblood |
| Version Model Number | LRW-50-07-PS |
| Company DUNS | 658873912 |
| Company Name | PURIBLOOD MEDICAL CO., LTD. |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04719878520508 [Primary] |
| GS1 | 14719878520505 [Package] Contains: 04719878520508 Package: carton [25 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 | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-26 |
| Device Publish Date | 2024-02-16 |
| 14719878520512 | LRW-50-08-PS |
| 14719878520505 | LRW-50-07-PS |
| 14719878520499 | LRW-50-06-PS |
| 14719878520482 | LRW-50-05-PS |
| 14719878520475 | LRW-50-04-PS |
| 14719878520468 | LRW-50-01-PS |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PURIBLOOD 98067852 not registered Live/Pending |
PURIBLOOD MEDICAL CO., LTD. 2023-06-30 |
![]() PURIBLOOD 87195253 5353270 Live/Registered |
PURIBLOOD MEDICAL CO., LTD. 2016-10-06 |