| Primary Device ID | 00724995209131 |
| NIH Device Record Key | 47252dec-38b4-42fc-820f-3edf1e002cc3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ArConnect |
| Version Model Number | Combo Probe ArConnect |
| Catalog Number | G1140006 |
| Company DUNS | 627879687 |
| Company Name | US Endoscopy |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx | |
| Phone | +1(800)548-4873 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00724995209131 [Primary] |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-08-29 |
| Device Publish Date | 2022-08-19 |
| 10724995180284 | The ArConnect argon probe connector allows the delivery of monopolar high frequency electrosurgi |
| 00724995209131 | The ArConnect Argon Combo Probe 3.2, 220 ArConnect is for the exclusive use with the gi4000 Ele |
| 00724995209124 | The ArConnect Argon Combo Probe 2.3, 330 ArConnect is for the exclusive use with the gi4000 Ele |
| 00724995209117 | The ArConnect Combo Probe 2.3, 220 ArConnect is for the exclusive use with the gi4000 Electrosur |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ARCONNECT 98459509 not registered Live/Pending |
Diversified Labeling Solutions, Inc. 2024-03-20 |
![]() ARCONNECT 85266984 4147662 Live/Registered |
UNITED STATES ENDOSCOPY GROUP, INC. 2011-03-15 |
![]() ARCONNECT 79322656 not registered Live/Pending |
Glaswerke Arnold GmbH & Co. KG 2021-07-15 |
![]() ARCONNECT 76428075 2790506 Dead/Cancelled |
HARBOR PAYMENTS CORPORATION 2002-07-08 |