Primary Device ID | 00860624000462 |
NIH Device Record Key | e57f4772-9f59-4f59-aef7-86e2a0e2f717 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AURORA Surgiscope |
Version Model Number | AS8/70 |
Catalog Number | AS8/70 |
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 |
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Length | 70 Millimeter |
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Length | 70 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860624000462 [Primary] |
GWG | Endoscope, Neurological |
GZT | Retractor, Self-Retaining, For Neurosurgery |
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 |