Home Monitoring Service Center 448495

GUDID 04035479166106

BIOTRONIK SE & Co. KG

Patient health record information system
Primary Device ID04035479166106
NIH Device Record Key4013ad49-7dfd-4cea-8719-46aa5a545f53
Commercial Distribution StatusIn Commercial Distribution
Brand NameHome Monitoring Service Center
Version Model Number3.44
Catalog Number448495
Company DUNS315620229
Company NameBIOTRONIK SE & Co. KG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)345-0374
Emailjon.brumbaugh@biotronik.com
Phone+1(888)345-0374
Emailjon.brumbaugh@biotronik.com
Phone+1(888)345-0374
Emailjon.brumbaugh@biotronik.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104035479166106 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OSRPacemaker/icd/crt non-implanted components

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-07-03
Device Publish Date2019-06-25

On-Brand Devices [Home Monitoring Service Center]

040354791617503.43
040354791661063.44
040354791664033.45
040354791674933.46
040354791675093.47
040354791687733.48
040354791694663.49
040354791617433.42
040354791582483.38
040354791524133.35
040354791488673.33
040354791488433.31
040354791442583.29
076401304573003.50
040354791755593.51
040354791765873.53
040354791779423.54
040354791797793.55
040354791820453.57
040354791832643.58
040354791861283.60
040354791871633.61
040354791846363.59
040354791761433.50

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