| Primary Device ID | 00880304451759 |
| NIH Device Record Key | da40f6db-2c7a-4b1e-b35b-a83eb4c82954 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BMA Kit |
| Version Model Number | 800-0705 |
| Catalog Number | 800-0705 |
| Company DUNS | 802003074 |
| Company Name | Biomet Biologics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304451759 [Primary] |
| LWE | Bone marrow collection/transfusion kit |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-11 |
| Device Publish Date | 2019-02-22 |
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| 00880304460652 - GPS® III | 2020-02-05 |
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| 00880304681484 - BioCUE® Concentration System | 2020-01-24 |
| 00880304680333 - PERFUSE DECOMPRESSION INSTRUMENTATION | 2019-08-09 |
| 00880304400085 - Biomet® | 2019-06-19 |
| 00880304400092 - Plasmax® Counterbalance | 2019-06-19 |