SureTip

GUDID 00850013050123

SureTip, GEN, 10mm, straight tip

Clinicon 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
Primary Device ID00850013050123
NIH Device Record Key16f79b62-33ac-40d0-844b-619ca8c6498e
Commercial Distribution StatusIn Commercial Distribution
Brand NameSureTip
Version Model Number3728
Company DUNS785275777
Company NameClinicon 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 Batchfalse
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100850013050123 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-13
Device Publish Date2021-05-05

Devices Manufactured by Clinicon Corporation

00850013050154 - SureGuide2021-05-14 SureGuide, 2.00m Fiber Cable Assembly, SMA Connector with Interlock Wire
00850013050161 - SureGuide2021-05-14 SureGuide, 2.00m Fiber Cable Assembly, ST Connector
00850013050178 - SureGuide2021-05-14 SureGuide, 2.75m Fiber Cable Assembly,SMA with Interlock Wire
00850013050185 - SureGuide2021-05-14 SureGuide, 2.75m Fiber Cable Assembly, ST Connector
00850013050000 - SureProbe2021-05-13 SureProbe, Neuro, 40mm Straight Dissecting Tip Assembly
00850013050017 - SureProbe2021-05-13 SureProbe, Neuro, 50mm Straight Dissecting Tip Assembly
00850013050024 - SureProbe2021-05-13 SureProbe, Neuro, 80mm Straight Dissecting Tip Assembly Copy
00850013050031 - SureProbe2021-05-13 SureProbe, ENT, 50mm, Nasal Straight Dissecting Tip Assembly

Trademark Results [SureTip]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SURETIP
SURETIP
85024442 not registered Dead/Abandoned
Fritz A. Brauer
2010-04-27

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