Primary Device ID | 07290109180809 |
NIH Device Record Key | 81154bef-683d-4862-a7e4-72142aa7ae06 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterile Clear Sleeve,10 pack |
Version Model Number | KIT0742-01 |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +97246187100 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109180809 [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 | 3 |
Public Version Date | 2018-11-08 |
Device Publish Date | 2017-01-17 |
07290109181141 | Sterile Clear Sleeve,10 pack |
07290109180809 | KIT0742-01 |
07290109184975 | KIT0742-03 |
07290115750850 | KIT0742-04 |
07290115752212 | KIT0742-05 |