NanoSurge

GUDID 00877972005995

GENICON, INC.

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
Primary Device ID00877972005995
NIH Device Record Key045cc4d2-affd-4336-a902-d26884470199
Commercial Distribution StatusIn Commercial Distribution
Brand NameNanoSurge
Version Model Number528-063-945
Company DUNS079805400
Company NameGENICON, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100877972005995 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEACannula, Surgical, General & Plastic Surgery

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-01-09
Device Publish Date2017-05-05

On-Brand Devices [NanoSurge]

00877972006251520-063-950
00877972006237520-063-945
00877972006213520-063-920
00877972006190520-063-910
00877972006015528-063-950
00877972005995528-063-945
00877972005971528-063-920
00877972005957528-063-910

Trademark Results [NanoSurge]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NANOSURGE
NANOSURGE
77375118 not registered Dead/Abandoned
Mutual Pharmaceutical Co., Inc.
2008-01-18

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