Primary Device ID | 08100410603357 |
NIH Device Record Key | 3ac6fbc7-e9ca-4a2c-a709-0e68108e0180 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arthrocare |
Version Model Number | EICA8870-01 |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08100410603357 [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 | 2019-12-13 |
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 |