LIGHT GUIDE 7205178

GUDID 03596010373236

LT GUIDE GEMINI 5MM X 10FT

Smith & Nephew, Inc.

Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor
Primary Device ID03596010373236
NIH Device Record Key163a0b23-d4a7-45e6-9a56-18ec1d6efde2
Commercial Distribution StatusIn Commercial Distribution
Brand NameLIGHT GUIDE
Version Model Number7205178
Catalog Number7205178
Company DUNS045483575
Company NameSmith & Nephew, 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 Usefalse
Lot Batchtrue
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(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS103596010373236 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


[03596010373236]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-09-07
Device Publish Date2017-11-13

On-Brand Devices [LIGHT GUIDE]

03596010373236LT GUIDE GEMINI 5MM X 10FT
03596010103246LIGHT CABLE GEMINI 5MM X 8FT

Trademark Results [LIGHT GUIDE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LIGHT GUIDE
LIGHT GUIDE
79144663 4701858 Live/Registered
SES-imagotag Deutschland GmbH
2013-12-13

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