Entovis SR 371993

GUDID 04035479115180

BIOTRONIK SE & Co. KG

Single-chamber implantable pacemaker, rate-responsive
Primary Device ID04035479115180
NIH Device Record Key0770c12c-4bf2-448f-9ac3-aed502717f7b
Commercial Distribution StatusIn Commercial Distribution
Brand NameEntovis SR
Version Model Number371993
Catalog Number371993
Company DUNS315620229
Company NameBIOTRONIK SE & Co. KG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains 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
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
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
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
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
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
Phone+1(888)345-0374
Emailjon.brumbaugh@biotronik.com

Operating and Storage Conditions

Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit
Storage Environment TemperatureBetween 14 Degrees Fahrenheit and 113 Degrees Fahrenheit

Device Identifiers

Device Issuing AgencyDevice ID
GS104035479115180 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NVZPulse generator, permanent, implantable

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-02-05
Device Publish Date2014-08-19

Devices Manufactured by BIOTRONIK SE & Co. KG

04035479001575 - M-502024-10-24
04035479176143 - Home Monitoring Service Center2024-09-30
04035479184636 - Home Monitoring Service Center2024-09-23
04035479187163 - Home Monitoring Service Center2024-09-11
04035479186005 - NEO2024-06-25
04035479186012 - PSW2024-06-25
04035479052515 - PK-222 US/2,8m2024-06-06
04035479186128 - Home Monitoring Service Center2024-06-06

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.