Primary Device ID | 07290109184364 |
NIH Device Record Key | 3a5bf358-d40e-43c3-8454-0fcaa59f9aa4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterile Cover For Device, 10 pack |
Version Model Number | KIT0136-03 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | 07290109184364 [Primary] |
HAW | Neurological Stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-05 |
Device Publish Date | 2020-07-28 |
07290109181332 | KIT0136-02 |
07290109184364 | KIT0136-03 |
07290109184586 | KIT0136-04 |