| Primary Device ID | 05714188308067 |
| NIH Device Record Key | 54e412ba-25db-41f0-8c03-1fc7af81b1d6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 3CP™ Centrifuge Kit |
| Version Model Number | 1 |
| Company DUNS | 312293991 |
| Company Name | Reapplix ApS |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 4588168066 |
| info@reapplix.com | |
| Phone | 4588168066 |
| info@reapplix.com | |
| Phone | 4588168066 |
| info@reapplix.com | |
| Phone | 4588168066 |
| info@reapplix.com | |
| Phone | 4588168066 |
| info@reapplix.com | |
| Phone | 4588168066 |
| info@reapplix.com | |
| Phone | 4588168066 |
| info@reapplix.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05714188308067 [Primary] |
| PMQ | Peripheral Blood Processing Device For Wound Management |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-11 |
| Device Publish Date | 2019-04-03 |
| 05714188308050 | Kit that includes 3CP Centrifuge, power cord, external power supply, 3CP Counterbalance, bag wit |
| 05714188308067 | Kit that includes 3CP Centrifuge, power cord, external power supply, 3CP Counterbalance, bag wit |
| 05714188308005 | Kit that includes 3CP Centrifuge, power cord, external power supply, 3CP Counterbalance, bag wit |