Primary Device ID | 07290109181110 |
NIH Device Record Key | acd74396-e6ac-4b96-b050-0cf305afc565 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mazor X Spine Disposable Kit |
Version Model Number | KIT0574-05 |
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 | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +97246187100 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109181110 [Primary] |
OLO | Orthopedic Stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-02-14 |
07290109183268 | KIT0574-06 |
07290109181110 | Mazor X Spine Disposable Kit |
07290109181011 | Mazor X Spine Disposable Kit |
07290109184494 | KIT0574-07 |
07290115750881 | KIT0574-08 |
07290115752786 | KIT0574-10 |
07290115753141 | KIT0574-11 |