Primary Device ID | 10845854850312 |
NIH Device Record Key | 8a2b8eea-8524-4f1e-a17e-86d316664814 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | W2000 |
Catalog Number | W2000 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854850312 [Direct Marking] |
GS1 | 20845854850319 [Primary] |
HRX | Arthroscope |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-17 |
Device Publish Date | 2018-08-17 |
30653405990486 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 15MM, TITANIUM |
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30653405990547 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 20MM, TITANIUM |
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