Primary Device ID | 07290109182049 |
NIH Device Record Key | e38fdb3f-86e3-466a-bbbb-6181efe9e98d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dual Clamp |
Version Model Number | MAS1355-05 |
Catalog Number | MAS1355-05S |
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 | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109182049 [Primary] |
OLO | Orthopedic Stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07290109182049]
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Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-01-30 |
Device Publish Date | 2018-12-03 |
07290109182049 | MAS1355-05 |
07290115750652 | MAS1355-06S |
07290115751758 | MAS1355-07S |