Primary Device ID | 04035479166106 |
NIH Device Record Key | 4013ad49-7dfd-4cea-8719-46aa5a545f53 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Home Monitoring Service Center |
Version Model Number | 3.44 |
Catalog Number | 448495 |
Company DUNS | 315620229 |
Company Name | BIOTRONIK SE & Co. KG |
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 | false |
Manufacturing Date | false |
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 |
Phone | +1(888)345-0374 |
jon.brumbaugh@biotronik.com | |
Phone | +1(888)345-0374 |
jon.brumbaugh@biotronik.com | |
Phone | +1(888)345-0374 |
jon.brumbaugh@biotronik.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04035479166106 [Primary] |
OSR | Pacemaker/icd/crt non-implanted components |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-03 |
Device Publish Date | 2019-06-25 |
04035479161750 | 3.43 |
04035479166106 | 3.44 |
04035479166403 | 3.45 |
04035479167493 | 3.46 |
04035479167509 | 3.47 |
04035479168773 | 3.48 |
04035479169466 | 3.49 |
04035479161743 | 3.42 |
04035479158248 | 3.38 |
04035479152413 | 3.35 |
04035479148867 | 3.33 |
04035479148843 | 3.31 |
04035479144258 | 3.29 |
07640130457300 | 3.50 |
04035479175559 | 3.51 |
04035479176587 | 3.53 |
04035479177942 | 3.54 |
04035479179779 | 3.55 |
04035479182045 | 3.57 |
04035479183264 | 3.58 |
04035479186128 | 3.60 |
04035479187163 | 3.61 |
04035479184636 | 3.59 |
04035479176143 | 3.50 |