NaviPro™

GUDID 08714729839910

Lake Region Medical

Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use Gastro-urological guidewire, single-use
Primary Device ID08714729839910
NIH Device Record Key62b6f737-1789-4fec-8de8-5fadfcedb67b
Commercial Distribution StatusIn Commercial Distribution
Brand NameNaviPro™
Version Model NumberM00556230
Company DUNS031108704
Company NameLake Region Medical
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 Batchtrue
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 Dimensions

Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry, dark place.

Device Identifiers

Device Issuing AgencyDevice ID
GS108714729839910 [Package]
Contains: 08714729848226
Package: [5 Units]
In Commercial Distribution
GS108714729848226 [Primary]

FDA Product Code

OCYEndoscopic Guidewire, Gastroenterology-Urology

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-12-06
Device Publish Date2016-10-28

On-Brand Devices [NaviPro™]

08714729839927M00556240
08714729839934M00556250
08714729839903M00556220
08714729839910M00556230
08714729839880M00556200
08714729839897M00556210
8714729839866M00556180
08714729839873M00556190

Trademark Results [NaviPro]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NAVIPRO
NAVIPRO
85822792 4593675 Live/Registered
ADVICENT SOLUTIONS, LP
2013-01-14
NAVIPRO
NAVIPRO
85812072 4569095 Live/Registered
Boston Scientific Scimed, Inc.
2012-12-28
NAVIPRO
NAVIPRO
79062128 3718789 Dead/Cancelled
Gábor Borsik
2008-10-20
NAVIPRO
NAVIPRO
79062128 3718789 Dead/Cancelled
Gábor Müller
2008-10-20
NAVIPRO
NAVIPRO
78707698 not registered Dead/Abandoned
Ten Technology, Inc.
2005-09-06
NAVIPRO
NAVIPRO
78097324 2830739 Live/Registered
KINAMED NAVIGATION SYSTEMS, LLC
2001-12-07
NAVIPRO
NAVIPRO
75315200 not registered Dead/Abandoned
TEXAS INSTRUMENTS INCORPORATED
1997-06-26

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