| Primary Device ID | 07290109181325 |
| NIH Device Record Key | 8d88a558-77e5-4b18-8be8-ce70a0c2c27d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SA Reduction Tube, 10 pack |
| Version Model Number | KIT0142-03 |
| Company DUNS | 532681590 |
| Company Name | MAZOR ROBOTICS LTD |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290109181325 [Primary] |
| OLO | Orthopedic Stereotaxic Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07290109181325]
Moist Heat or Steam Sterilization
[07290109181325]
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[07290109181325]
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[07290109181325]
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[07290109181325]
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[07290109181325]
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[07290109181325]
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[07290109181325]
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[07290109181325]
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[07290109181325]
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| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-06-08 |
| Device Publish Date | 2018-02-28 |
| 07290109183312 | KIT0142-04 |
| 07290109181325 | KIT0142-03 |
| 07290109180175 | KIT0142-02 |
| 07290115750027 | KIT0142-05 |
| 07290115750904 | KIT0142-06 |
| 07290115752779 | KIT0142-08 |