INTREPID®

GUDID 00380657510139

INTREPID® Micro-Coaxial I/A tip, 0.3 mm, Bent

Alcon Laboratories, Inc.

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
Primary Device ID00380657510139
NIH Device Record Keyceb99e4a-9973-477c-886a-eee5cbb83144
Commercial Distribution StatusIn Commercial Distribution
Brand NameINTREPID®
Version Model Number8065751013
Company DUNS008018525
Company NameAlcon Laboratories, Inc.
Device Count1
DM Exempttrue
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100380657510139 [Primary]

FDA Product Code

NKKNEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


[00380657510139]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-10
Device Publish Date2020-09-02

On-Brand Devices [INTREPID®]

10380657528858INTREPID® Transformer IA HP
00380657510139INTREPID® Micro-Coaxial I/A tip, 0.3 mm, Bent
00380657510122INTREPID® Micro-Coaxial I/A tip, 0.3 mm, Straight

Trademark Results [INTREPID]

Mark Image

Registration | Serial
Company
Trademark
Application Date
INTREPID
INTREPID
98432091 not registered Live/Pending
INTREPID IP HOLDINGS PTY LTD
2024-03-04
INTREPID
INTREPID
98339923 not registered Live/Pending
Intrepid Industries Inc.
2024-01-03
INTREPID
INTREPID
98165319 not registered Live/Pending
CHA Consulting, Inc.
2023-09-05
INTREPID
INTREPID
98009011 not registered Live/Pending
Rutena Freezone NV
2023-05-23
INTREPID
INTREPID
97918450 not registered Live/Pending
Sheltered Wings, Inc.
2023-05-03
INTREPID
INTREPID
97604853 not registered Live/Pending
Alliance Sports Group, L.P.
2022-09-23
INTREPID
INTREPID
97150660 not registered Live/Pending
MTS Systems Corporation
2021-12-01
INTREPID
INTREPID
90540964 not registered Live/Pending
Bulletproof Property Management, LLC
2021-02-23
INTREPID
INTREPID
90530357 not registered Live/Pending
Intrepid Protect Inc.
2021-02-16
INTREPID
INTREPID
90197339 not registered Live/Pending
"INTERPIPE UKRAINE" LIMITED LIABILITY COMPANY
2020-09-21
INTREPID
INTREPID
88889806 not registered Live/Pending
Langtry Farms, LLC
2020-04-27
INTREPID
INTREPID
88788253 not registered Live/Pending
True IP, LLC
2020-02-06

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