| Primary Device ID | 08714729452270 | 
| NIH Device Record Key | 7f5bdf75-1a47-45a5-961a-2758f92af121 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Blazer® II XP | 
| Version Model Number | M0044500TH0 | 
| Catalog Number | M0044500TH0 | 
| 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 | true | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | false | 
| 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 Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 08714729452270 [Primary] | 
| OAD | catheter, percutaneous, cardiac ablation, for treatment of atrial flutter | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 5 | 
| Public Version Date | 2021-09-16 | 
| Device Publish Date | 2014-09-24 | 
| 08714729452416 | Temperature Ablation Catheter | 
| 08714729452409 | Temperature Ablation Catheter | 
| 08714729452393 | Temperature Ablation Catheter | 
| 08714729452386 | Temperature Ablation Catheter | 
| 08714729452379 | Temperature Ablation Catheter | 
| 08714729452362 | Temperature Ablation Catheter | 
| 08714729452355 | Temperature Ablation Catheter | 
| 08714729452348 | Temperature Ablation Catheter | 
| 08714729452331 | Temperature Ablation Catheter | 
| 08714729452324 | Temperature Ablation Catheter | 
| 08714729452317 | Temperature Ablation Catheter | 
| 08714729452300 | Temperature Ablation Catheter | 
| 08714729452294 | Temperature Ablation Catheter | 
| 08714729452287 | Temperature Ablation Catheter | 
| 08714729452270 | Temperature Ablation Catheter | 
| 08714729144335 | Temperature Ablation Catheter | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  BLAZER  98889724  not registered Live/Pending | Hofmann Fluid Power, Inc. 2024-12-06 | 
|  BLAZER  98535847  not registered Live/Pending | Rotary Digital LLC 2024-05-06 | 
|  BLAZER  98440727  not registered Live/Pending | Dong Yongqiang 2024-03-08 | 
|  BLAZER  97855247  not registered Live/Pending | ROCKY MCCORKLE LLC 2023-03-24 | 
|  BLAZER  90531837  not registered Live/Pending | BPB, Inc 2021-02-17 | 
|  BLAZER  90355980  not registered Live/Pending | Beam Of Light Technologies, Inc. 2020-12-03 | 
|  BLAZER  88699512  not registered Live/Pending | Bohning Company Ltd. 2019-11-20 | 
|  BLAZER  88530523  not registered Live/Pending | Sapphire Scientific, Inc. 2019-07-23 | 
|  BLAZER  88081581  not registered Live/Pending | Blazer Products, Incorporated 2018-08-16 | 
|  BLAZER  87825497  not registered Dead/Abandoned | Top Tobacco, LP 2018-03-08 | 
|  BLAZER  87214360  not registered Live/Pending | HANGZHOU HIKVISION DIGITAL TECHNOLOGY CO., LTD 2016-10-25 | 
|  BLAZER  87202115  not registered Dead/Abandoned | Iown LLC 2016-10-13 |