Virtuosaph Plus with Radial Indication

GUDID 50699753450764

Terumo Cardiovascular Systems Corporation

Endoscopic electrosurgical electrode, bipolar, single-use Endoscopic electrosurgical electrode, bipolar, single-use
Primary Device ID50699753450764
NIH Device Record Key1920153d-4c71-44d3-ac91-fe31566f0c26
Commercial Distribution StatusIn Commercial Distribution
Brand NameVirtuosaph Plus with Radial Indication
Version Model NumberVSP550EX
Company DUNS177655466
Company NameTerumo Cardiovascular Systems Corporation
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100699753450769 [Primary]
GS150699753450764 [Package]
Contains: 00699753450769
Package: 5 Piece Case [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-02-07
Device Publish Date2016-10-12

Devices Manufactured by Terumo Cardiovascular Systems Corporation

50699753531210 - Cardiovascular Procedure Kit2024-04-19
50699753531227 - Cardiovascular Procedure Kit2024-04-19
50699753531234 - Cardiovascular Procedure Kit2024-04-19
50699753531180 - Cardiovascular Procedure Kit2024-04-18
00699753531192 - Cardiovascular Procedure Kit2024-04-18
00699753531208 - Cardiovascular Procedure Kit2024-04-18
50699753531104 - Cardiovascular Procedure Kit2024-04-15
50699753531111 - Cardiovascular Procedure Kit2024-04-15

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