Primary Device ID | 14719878520499 |
NIH Device Record Key | 02e81ee0-b500-46c0-b3da-0a240bb8d5f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Puriblood |
Version Model Number | LRW-50-06-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 | 04719878520492 [Primary] |
GS1 | 14719878520499 [Package] Contains: 04719878520492 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 |