Primary Device ID | 08714729861980 |
NIH Device Record Key | c20cdb6a-9b0e-4387-b915-d70a78bc050b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Maestro 4000™ Pod, 100W |
Version Model Number | M0044010R0 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729861980 [Primary] |
OAD | catheter, percutaneous, cardiac ablation, for treatment of atrial flutter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2022-06-10 |
Device Publish Date | 2015-01-27 |
08714729861997 | RF Cardiac Ablation Pod, 100W |
08714729861980 | RF Cardiac Ablation Pod, 100W |
08714729861966 | RF Cardiac Ablation Pod, 100W |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MAESTRO 4000 85879149 4813276 Live/Registered |
Boston Scientific Scimed, Inc. 2013-03-18 |