Primary Device ID | 00857676008188 |
NIH Device Record Key | 40fab34b-51bd-4f7d-931c-83ce32b5a38e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arthrex |
Version Model Number | 2.4 mm Volar Distal Radius Plate Template |
Catalog Number | AR-8924VT-S |
Company DUNS | 084330422 |
Company Name | Eca Medical Instruments |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857676008188 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-05 |
Device Publish Date | 2023-03-28 |
00857676008195 | 2.4 mm Volar Distal Radius Removal Driver |
00857676008188 | 2.4 mm Volar Distal Radius Plate Template |
00857676008171 | 2.4 mm Volar Distal Radius Instrument System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ARTHREX 87595305 5598566 Live/Registered |
Arthrex, Inc. 2017-09-04 |
ARTHREX 87595302 5598565 Live/Registered |
Arthrex, Inc. 2017-09-04 |
ARTHREX 85078407 3911238 Live/Registered |
Arthrex, Inc. 2010-07-06 |
ARTHREX 74317485 1788030 Live/Registered |
ARTHREX INC. 1992-09-24 |
ARTHREX 74128118 not registered Dead/Abandoned |
Arthrex Arthroscopy Instruments, Inc. 1991-01-04 |
ARTHREX 73436631 1328327 Dead/Cancelled |
Surgical Equipment Associates, Ltd. 1983-07-28 |
ARTHREX 73281788 1191044 Dead/Cancelled |
Gerchenson; Emile H. 1980-10-14 |