PSW 403222

GUDID 04035479140380

BIOTRONIK SE & Co. KG

Cardiac pulse generator programmer
Primary Device ID04035479140380
NIH Device Record Key69635cd3-843a-44e8-9d8c-fe3bf9ae2e42
Commercial Distribution Discontinuation2020-10-16
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePSW
Version Model Number1307.U
Catalog Number403222
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
GS104035479140380 [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 StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-10-19
Device Publish Date2014-08-21

On-Brand Devices [PSW]

040354791663971904.U
040354791576921703.U
040354791576781702.U
040354791541651506.U/1
040354791527651507.U
040354791502041502.U
040354791492601501.U
040354791471431403.U
040354791406701304.U
040354791403801307.U
040354791518431506.U
040354791502111503.U
040354791747982100.U
040354791608381801.U
040354791577081704.U
040354791620471802.U
040354791644231901.U
040354791644161804.U
040354791780242201.U/1
040354791815432301.U
040354791796322204.U
040354791842922303.U
040354791860122401.U

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