Home Monitoring Service Center 419322

GUDID 04035479152413

BIOTRONIK SE & Co. KG

Patient health record information system
Primary Device ID04035479152413
NIH Device Record Key4fca4f28-64c4-44c2-b0c9-ed54d8c8cca7
Commercial Distribution Discontinuation2020-10-16
Commercial Distribution StatusNot in Commercial Distribution
Brand NameHome Monitoring Service Center
Version Model Number3.35
Catalog Number419322
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104035479152413 [Primary]

FDA Product Code

OSRPacemaker/icd/crt non-implanted components

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-10-19
Device Publish Date2016-08-29

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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