N/A 000150

GUDID 20653405050855

Marked Spring Tip Guidewire

Conmed Corporation

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Primary Device ID	20653405050855
NIH Device Record Key	59fa82a0-2040-4276-a7b4-dfefd5d35e51
Commercial Distribution Status	In Commercial Distribution
Brand Name	N/A
Version Model Number	000150
Catalog Number	000150
Company DUNS	071595540
Company Name	Conmed Corporation
Device Count	2
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	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM
Phone	+1(800)237-0169
Email	CUSTOMER_SERVICE@CONMED.COM

Device Dimensions

Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter
Length	210 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00653405050851 [Unit of Use]
GS1	10653405050858 [Primary]
GS1	20653405050855 [Package] Contains: 10653405050858 Package: BOX [2 Units] In Commercial Distribution
GS1	30653405050852 [Direct Marking]

FDA Product Code

KNQ	Dilator, esophageal

Sterilization

Steralize Prior To Use	true
Device Is Sterile	false

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

[20653405050855]

Ethylene Oxide

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2022-03-23
Device Publish Date	2016-09-24

On-Brand Devices [N/A]

20653405050855	Marked Spring Tip Guidewire
10653405053699	CONMED Endoscopic Overtube