Primary Device ID | 00889095998696 |
NIH Device Record Key | 103cae8d-5b29-44ed-8262-893703dfc849 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CROSSWAY |
Version Model Number | 6177.2111 |
Company DUNS | 139105691 |
Company Name | GLOBUS MEDICAL, INC. |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
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 | +1(610)930-1800 |
info@globusmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889095998696 [Primary] |
HRX | Arthroscope |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889095998696]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2019-07-12 |
00889095998696 | Adjustable Depth Stop, 18-26mm |
00889095998689 | Harvesting Mill, 6mm |
00889095998634 | Temporary Fixation Screw, 10mm |
00889095741025 | Adjustable Depth Stop, 10-18mm |
00889095740998 | Channel Guide, Right 10° |
00889095740981 | Adjustable Channel Guide |
00889095740974 | Channel Guide, Left 10° |
00889095740929 | Fixation Screw Driver |
00889095998672 | Pilot Drill, 2mm |
00889095998658 | Temporary Fixation Screw, 14mm |
00889095998641 | Temporary Fixation Screw, 12mm |
00889095998665 | Temporary Fixation Screw, 16mm |