| Primary Device ID | 00860624000455 |
| NIH Device Record Key | 89abfeaa-8080-4f81-b2fb-503ca9190d29 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AURORA Surgiscope |
| Version Model Number | AS8/100 |
| Catalog Number | AS8/100 |
| Company DUNS | 080909607 |
| Company Name | REBOUND THERAPEUTICS CORPORATION |
| 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 | 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)654-2873 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860624000455 [Primary] |
| GTZ | ANTISERA, ALL GROUPS, STREPTOCOCCUS SPP. |
| GWG | Endoscope, Neurological |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-12-26 |
| Device Publish Date | 2019-12-18 |
| 00860624000448 | The AURORA Surgiscope System consists of two components: sterile, single use, neurological endo |
| 00860624000462 | The AURORA Surgiscope System consists of two components: sterile, single use, neurological endo |
| 00860624000455 | The AURORA Surgiscope System consists of two components: sterile, single use, neurological endo |
| 00850002332131 | The AURORA Surgiscope System consists of two components: sterile, single use, neurological endo |