Patient Cables

GUDID 90817266020832

5 Lead Patient Trunk Cable

MERIT CABLES INCORPORATED

Electrical-only medical device connection cable, reusable

• Primary Device ID: 90817266020832
• NIH Device Record Key: fbc41b60-6d71-4295-bb52-ea98c112a98d
• Commercial Distribution Discontinuation: 2018-03-23
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Patient Cables
• Version Model Number: 73585
• Company DUNS: 180587883
• Company Name: MERIT CABLES INCORPORATED
• 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: false
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com
• Phone: 714-918-1935
• Email: rmauricio@meritcables.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	90817266020832 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K942321

FDA Product Code

• DSA: Cable, Transducer And Electrode, Patient, (Including Connector)

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-04-23
• Device Publish Date: 2018-03-23

On-Brand Devices [Patient Cables]

• 90817266020832: 5 Lead Patient Trunk Cable
• 90817266020542: Patient Cable Non Detachable 5 Lead