BIOSNDSTR10G

GUDID 10888551007122

CATHETER SOUNDSTAR 3D DIAGNOSTIC ULTRASOUND 10FR FOR USE ON GE IMAGING SYSTEM

STERILMED, INC.

Intracardiac ultrasound imaging catheter, steerable, reprocessed Intracardiac ultrasound imaging catheter, steerable, reprocessed
Primary Device ID10888551007122
NIH Device Record Key22ea1765-2af2-415a-82af-d5b211eaa031
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberBIOSNDSTR10G
Catalog NumberBIOSNDSTR10G
Company DUNS175899459
Company NameSTERILMED, INC.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110888551007122 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OWQReprocessed intravascular ultrasound catheter

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10888551007122]

Ethylene Oxide


[10888551007122]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-03-21
Device Publish Date2016-09-22

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10888551045209 - NA2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
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