Circulo 15R2011-06-002

GUDID 00816349012662

Lake Region Medical

Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use
Primary Device ID00816349012662
NIH Device Record Key7e5644bb-2962-4738-a5e4-e897ee087637
Commercial Distribution StatusIn Commercial Distribution
Brand NameCirculo
Version Model NumberDAIBW-001
Catalog Number15R2011-06-002
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 Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter
Outer Diameter35 Inch
Length275 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100816349012662 [Primary]
GS110816349012669 [Package]
Package: [5 Units]
In Commercial Distribution

FDA Product Code

DQXWire, Guide, Catheter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-21
Device Publish Date2022-10-13

On-Brand Devices [Circulo ]

10816349012683DAIBW-003
00816349012662DAIBW-001

Trademark Results [Circulo]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CIRCULO
CIRCULO
97342512 not registered Live/Pending
St. Jude Medical, Cardiology Division, Inc.
2022-04-01
CIRCULO
CIRCULO
97312417 not registered Live/Pending
Circulo, Inc.
2022-03-15
CIRCULO
CIRCULO
74016668 not registered Dead/Abandoned
Industria De Linhas Leopoldo Schmalz S.A.
1990-01-05
CIRCULO
CIRCULO
73385243 1258585 Dead/Cancelled
Industria de Linhas Leopoldo Schmalz S.A.
1982-09-13
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