Primary Device ID | 07290109181158 |
NIH Device Record Key | cb5bfeb8-74bd-4406-8de0-ee4b38a3fe70 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mazor X System |
Version Model Number | TPL0059-05 |
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 | false |
Lot Batch | false |
Serial Number | true |
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 |
Phone | +97246187100 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109181158 [Primary] |
OLO | Orthopedic Stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-02-18 |
07290109183213 | TPL0059-06 |
07290109181158 | TPL0059-05 |
07290109180465 | Mazor X System |
17290109180465 | TPL0059-03 |
07290109184838 | TPL0059-08 |
07290109184098 | TPL0059-07 |
07290115751376 | TPL0059-09 |