| Primary Device ID | B504TCAR65620 |
| NIH Device Record Key | c78c3a34-c007-4026-a7b4-a450b610449a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arthrex |
| Version Model Number | AR-6562 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| 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 |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.c | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.c |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504TCAR65620 [Primary] |
| NBH | Accessories, Arthroscopic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-09-27 |
| Device Publish Date | 2018-08-27 |
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 |