TrailBlazer™Angled

GUDID 20643169694938

ASC-035-135 FG ANGLED SUPPORT CATHETER

Covidien LP

Vascular guide-catheter, single-use

Primary Device ID	20643169694938
NIH Device Record Key	21987cac-25a5-48d9-a223-e249c2f706d8
Commercial Distribution Status	In Commercial Distribution
Brand Name	TrailBlazer™Angled
Version Model Number	ASC-035-135
Company DUNS	968903703
Company Name	Covidien LP
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com
Phone	+1(800)633-8766
Email	Corporate.UDI@medtronic.com

Device Dimensions

Catheter Gauge	4 French
Catheter Gauge	4 French
Catheter Gauge	4 French
Catheter Gauge	4 French
Catheter Gauge	4 French
Catheter Gauge	4 French
Catheter Gauge	4 French
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French
Length	135 Centimeter
Device Size Text, specify	0
Outer Diameter	1.04 Millimeter
Catheter Gauge	4 French

Operating and Storage Conditions

Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep away from sunlight
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169694934 [Primary]
GS1	20643169694938 [Package] Contains: 00643169694934 Package: PK [5 Units] In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K162384

FDA Product Code

DQY	CATHETER, PERCUTANEOUS

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	5
Public Version Date	2019-01-23
Device Publish Date	2016-10-22

On-Brand Devices [TrailBlazer™Angled]

20643169694945	ASC-035-150 FG ANGLED SUPPORT CATHETER
20643169694938	ASC-035-135 FG ANGLED SUPPORT CATHETER
20643169694921	ASC-035-090 FG ANGLED SUPPORT CATHETER
20643169694914	ASC-035-065 FG ANGLED SUPPORT CATHETER
20643169694907	ASC-018-150 FG ANGLED SUPPORT CATHETER
20643169694891	ASC-018-135 FG ANGLED SUPPORT CATHETER
20643169694884	ASC-018-090 FG ANGLED SUPPORT CATHETER
20643169694877	ASC-014-150 FG ANGLED SUPPORT CATHETER
20643169694860	ASC-014-135 FG ANGLED SUPPORT CATHETER
20643169694853	ASC-014-090 FG ANGLED SUPPORT CATHETER

Trademark Results [TrailBlazer]

Mark Image Registration \| Serial	Company Trademark Application Date
TRAILBLAZER 98469001 not registered Live/Pending	GROW COACHING SOLUTIONS, LLC 2024-03-26
TRAILBLAZER 98456859 not registered Live/Pending	Aurora Cooperative Elevator Company 2024-03-19
TRAILBLAZER 98385011 not registered Live/Pending	Generations of Sonoma, LLC 2024-01-31
TRAILBLAZER 98351133 not registered Live/Pending	Tarrant County College District 2024-01-10
TRAILBLAZER 98303111 not registered Live/Pending	TP-Holiday Group Limited 2023-12-07
TRAILBLAZER 98299673 not registered Live/Pending	Trailblazer Women's Wellness, PLLC 2023-12-05
TRAILBLAZER 98180580 not registered Live/Pending	Spinal Elements, Inc. 2023-09-14
TRAILBLAZER 97722935 not registered Live/Pending	Athletic Brewing Company LLC 2022-12-19
TRAILBLAZER 97670112 not registered Live/Pending	Trailblazer Energy Resources, LLC 2022-11-09
TRAILBLAZER 90787630 not registered Live/Pending	Made In Nature, LLC 2021-06-22
TRAILBLAZER 90274398 not registered Live/Pending	Intabio, Inc. 2020-10-23
TRAILBLAZER 88828665 not registered Live/Pending	eSite Analytics, Inc. 2020-03-10