Cragg-McNamara 41060-01

GUDID 00836462000308

Valved Infusion Catheter

Micro Therapeutics, Inc.

Peripheral vascular infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter

• Primary Device ID: 00836462000308
• NIH Device Record Key: 1667008a-ad8c-430b-96d3-f5be56af8c5d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cragg-McNamara
• Version Model Number: 41060-01
• Catalog Number: 41060-01
• Company DUNS: 826110710
• Company Name: Micro Therapeutics, Inc.
• 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: true
• 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(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Device Dimensions

• Device Size Text, specify: 0
• Length: 135 Centimeter
• Catheter Gauge: 5 French
• Device Size Text, specify: 0
• Length: 135 Centimeter
• Catheter Gauge: 5 French
• Device Size Text, specify: 0
• Length: 135 Centimeter
• Catheter Gauge: 5 French
• Device Size Text, specify: 0
• Length: 135 Centimeter
• Catheter Gauge: 5 French
• Device Size Text, specify: 0
• Length: 135 Centimeter
• Catheter Gauge: 5 French
• Device Size Text, specify: 0
• Length: 135 Centimeter
• Catheter Gauge: 5 French
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT
• Storage Environment Temperature: Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT
• Storage Environment Temperature: Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT
• Storage Environment Temperature: Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT
• Storage Environment Temperature: Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT
• Storage Environment Temperature: Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT
• Storage Environment Temperature: Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing Agency	Device ID
GS1	00836462000308 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K940634

FDA Product Code

• FOZ: Catheter, intravascular, therapeutic, short-term less than 30 days

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-04-09
• Device Publish Date: 2015-10-09

On-Brand Devices [Cragg-McNamara]

• 00836462000308: Valved Infusion Catheter
• 00836462000292: Valved Infusion Catheter
• 00836462000285: Valved Infusion Catheter
• 00836462000278: Valved Infusion Catheter
• 00836462000261: Valved Infusion Catheter
• 00836462000254: Valved Infusion Catheter
• 00836462000247: Valved Infusion Catheter
• 00836462000230: Valved Infusion Catheter
• 00836462000223: Valved Infusion Catheter
• 00836462000216: Valved Infusion Catheter
• 00836462000209: Valved Infusion Catheter
• 00836462000193: Valved Infusion Catheter
• 00836462000186: Valved Infusion Catheter
• 00836462000179: Valved Infusion Catheter
• 00836462000162: Valved Infusion Catheter
• 00836462000155: Valved Infusion Catheter
• 00836462000148: Valved Infusion Catheter
• 00836462000131: Valved Infusion Catheter
• 00836462000124: Valved Infusion Catheter
• 00836462000117: Valved Infusion Catheter
• 00836462000100: Valved Infusion Catheter
• 00836462000094: Valved Infusion Catheter
• 00836462000087: Valved Infusion Catheter
• 00836462000070: Valved Infusion Catheter
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• 00836462000056: Valved Infusion Catheter
• 00836462000049: Valved Infusion Catheter
• 00836462000032: Valved Infusion Catheter
• 00836462000025: Valved Infusion Catheter