Medtronic 990066

GUDID 07613327371260

EP CATHETER CABLE 8-PIN

STRYKER SUSTAINABILITY SOLUTIONS, INC.

Electrical-only medical device connection cable, reprocessed

• Primary Device ID: 07613327371260
• NIH Device Record Key: e833de9c-1fc8-4607-ab74-b7ea70d3e7b9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic
• Version Model Number: 990066
• Catalog Number: 990066
• Company DUNS: 020198912
• Company Name: STRYKER SUSTAINABILITY SOLUTIONS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: true
• 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(888)888-3433
• Email: RegulatoryAffairs2@stryker.com

Device Dimensions

• Length: 196 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327371260 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K030187

FDA Product Code

• DSA: CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-06-22

On-Brand Devices [Medtronic]

• 07613327469233: EP CATHETER CABLE 10-PIN
• 07613327371260: EP CATHETER CABLE 8-PIN