Primary Device ID | 07290109181394 |
NIH Device Record Key | 5e3f0894-4772-4a54-8a79-edbba7b2e7f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 360° Bridge |
Version Model Number | MAS2313-02 |
Catalog Number | KIT2313-01 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | 07290109181394 [Primary] |
OLO | Orthopedic Stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07290109181394]
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Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-22 |
Device Publish Date | 2021-03-14 |
07290109184142 | MAS2313-01 |
07290109181394 | MAS2313-02 |