| Primary Device ID | 08100410603241 |
| NIH Device Record Key | 9af2122c-e15e-4e97-82d2-3429f9ec5818 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arthrocare |
| Version Model Number | AC2430-01 |
| Catalog Number | AC1336-01 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| 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 | 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 | 08100410603241 [Primary] |
| NUJ | Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-03-09 |
| Device Publish Date | 2019-12-12 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ARTHROCARE 85707385 4548314 Live/Registered |
Bios Biochemicals Corp. 2012-08-19 |
![]() ARTHROCARE 78778510 3254296 Dead/Cancelled |
Schell & Kampeter, Inc. 2005-12-21 |
![]() ARTHROCARE 76250959 not registered Dead/Abandoned |
PHARMALIFE, INC. 2001-05-03 |
![]() ARTHROCARE 75034319 2015686 Live/Registered |
ArthroCare Corporation 1995-12-04 |