| Primary Device ID | 04035479135522 | 
| NIH Device Record Key | b327c6a0-844e-4150-bc56-b20e6c2dbc7f | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | BioMonitor | 
| Version Model Number | 2-AF | 
| Catalog Number | 398493 | 
| Company DUNS | 315620229 | 
| Company Name | BIOTRONIK SE & Co. KG | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Conditional | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | true | 
| Lot Batch | false | 
| Serial Number | true | 
| 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 Issuing Agency | Device ID | 
|---|---|
| GS1 | 04035479135522 [Primary] | 
| MXD | RECORDER,EVENT,IMPLANTABLE CARDIAC,(WITH ARRHYTHMIA DETECTION) | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 5 | 
| Public Version Date | 2020-01-09 | 
| Device Publish Date | 2016-04-29 | 
| 04035479158453 | III | 
| 04035479135539 | 2-S | 
| 04035479135522 | 2-AF | 
| 04035479131210 | 394119 | 
| 04035479144227 | Remote Assistant | 
| 04035479169862 | IIIm | 
| 04035479149314 | FIT-Fast Insert Tool 1 + 2, Set | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  BIOMONITOR  86538311  5046341 Live/Registered | BIOTRONIK SE & Co. KG 2015-02-18 | 
|  BIOMONITOR  79053841  3746900 Dead/Cancelled | BIOTRONIK SE & Co. KG 2008-01-30 | 
|  BIOMONITOR  79047745  3647657 Dead/Cancelled | BIOTRONIK SE & Co. KG 2007-11-01 | 
|  BIOMONITOR  78214992  2940748 Dead/Cancelled | Applera Corporation 2003-02-14 | 
|  BIOMONITOR  73014956  1016744 Dead/Expired | BIOCONTROL COMPANY 1974-03-04 |