Primary Device ID | 07290109181233 |
NIH Device Record Key | 9a1ccb6b-6aca-4451-aede-e3aaa197417f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Short Drill Guide and Short Cannula |
Version Model Number | KIT0737-02 |
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 | 07290109181233 [Primary] |
OLO | Orthopedic Stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07290109181233]
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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 |
07290109183305 | KIT0737-03 |
07290109181233 | KIT0737-02 |
07290109180755 | KIT0737-01 |
07290109184920 | KIT0737-04 |
07290115750805 | KIT0737-05 |
07290115752816 | KIT0737-07 |