LightTrail™ Single Use

GUDID 08714729939764

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 ID08714729939764
NIH Device Record Key9c161366-5c16-4c33-ae9e-17850175cc49
Commercial Distribution StatusIn Commercial Distribution
Brand NameLightTrail™ Single Use
Version Model NumberM0068F64500
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
GS108714729939764 [Primary]

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 Number2
Public Version Date2021-04-07
Device Publish Date2018-06-15

On-Brand Devices [LightTrail™ Single Use]

08714729939801Laser Fiber
08714729939795Laser Fiber
08714729939788Laser Fiber
08714729939771Laser Fiber
08714729939764Laser Fiber

Trademark Results [LightTrail]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LIGHTTRAIL
LIGHTTRAIL
85465838 4281502 Dead/Cancelled
BOSTON SCIENTIFIC LIMITED
2011-11-07
LIGHTTRAIL
LIGHTTRAIL
79373394 not registered Live/Pending
Boehringer Ingelheim International GmbH
2023-05-23

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