Flexiva™ ID

GUDID 08714729963820

High Power Single-Use Laser Fiber

BOSTON SCIENTIFIC CORPORATION

General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use General/multiple surgical laser system beam guide, single-use
Primary Device ID08714729963820
NIH Device Record Key0b983faf-a8a7-496b-a3b2-99e5678915e3
Commercial Distribution StatusIn Commercial Distribution
Brand NameFlexiva™ ID
Version Model NumberM006R8403940
Company DUNS021717889
Company NameBOSTON SCIENTIFIC 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

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Device Identifiers

Device Issuing AgencyDevice ID
GS108714729963813 [Primary]
GS108714729963820 [Package]
Contains: 08714729963813
Package: [5 Units]
In Commercial Distribution

FDA Product Code

GEXPowered laser surgical instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-04-07
Device Publish Date2017-10-21

On-Brand Devices [Flexiva™ ID]

08714729963820High Power Single-Use Laser Fiber
08714729963806High Power Single-Use Laser Fiber
08714729963783High Power Single-Use Laser Fiber
08714729963769High Power Single-Use Laser Fiber

Trademark Results [Flexiva]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FLEXIVA
FLEXIVA
85114331 4029813 Live/Registered
Boston Scientific Scimed, Inc.
2010-08-24

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