MPS Water Circuit Adapter, 16C

GUDID 20634624516117

QUEST MEDICAL INC

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• Primary Device ID: 20634624516117
• NIH Device Record Key: ddc2a767-7793-42cf-84da-f17dbcd389e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MPS Water Circuit Adapter, 16C
• Version Model Number: 5161110
• Company DUNS: 041810693
• Company Name: QUEST MEDICAL 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com
• Phone: 1-800-627-0226
• Email: custserv@questmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	20634624516117 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173716

FDA Product Code

• DTR: Heat-Exchanger, Cardiopulmonary Bypass

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: 2021-04-16
• Device Publish Date: 2021-04-08

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