VEQTRON

GUDID 06973031299719

Light Source

Guangdong Optomedic Technologies, Inc.

Stationary general-purpose fluoroscopic x-ray system, digital
Primary Device ID06973031299719
NIH Device Record Keyb8311fa5-dfdc-4e95-913d-7ae1fb257a90
Commercial Distribution StatusIn Commercial Distribution
Brand NameVEQTRON
Version Model Number71-182-30 NIR
Company DUNS544527790
Company NameGuangdong Optomedic Technologies, 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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106973031299719 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-20
Device Publish Date2023-11-11

Devices Manufactured by Guangdong Optomedic Technologies, Inc.

06973031299337 - 3D Laparoscope2024-08-23
06973031299344 - 3D Laparoscope2024-08-23
06973031299375 - Stellar Light Source 2024-08-23
06973031299382 - Stellar Exoscope2024-08-23
06973031299399 - Stellar 3D Fluorescence Camera Head2024-08-23
06973031299405 - Stellar 3D Camera Head2024-08-23
06973031299412 - Stellar Fluorescence Camera Head2024-08-23
06973031299429 - Stellar Camera Head2024-08-23

Trademark Results [VEQTRON]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VEQTRON
VEQTRON
97743382 not registered Live/Pending
AMNOTEC International Medical GmbH
2023-01-05

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