| Primary Device ID | 30812747016364 |
| NIH Device Record Key | ffb63115-e370-4443-83bb-2f7ec12c7b98 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HAEMONETICS CELL SAVER ELITE+ SYSTEM |
| Version Model Number | CSE-EW-US |
| Company DUNS | 057827420 |
| Company Name | HAEMONETICS CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| 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 | +1(800)-537-2802 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30812747016364 [Primary] |
| CAC | APPARATUS, AUTOTRANSFUSION |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-01-05 |
| 30812747016364 | CELL SAVER ELITE+ |