Mui Scientifc

GUDID 00678467503022

12-Channel HRM Colon Catheter (MMS-EM-3)

H & A Mui Enterprises Inc

Gastrointestinal manometric catheter, non-electronic

• Primary Device ID: 00678467503022
• NIH Device Record Key: 92abcb78-b445-4853-ad23-fcf9ac7a8637
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mui Scientifc
• Version Model Number: CR4-1040
• Company DUNS: 243872611
• Company Name: H & A Mui Enterprises 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com
• Phone: (905)-890-5525
• Email: mail@muiscientific.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00678467503022 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K983665

FDA Product Code

• KLA: Monitor, Esophageal Motility, And Tube

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: 2019-06-21
• Device Publish Date: 2019-06-13

Devices Manufactured by H & A Mui Enterprises Inc

• 00678467508102 - Mui Scientific: 2025-07-11 Single Use Esophageal 24 Channel Catheter
• 00678467508294 - Mui Scientific: 2025-07-11 Single Use Small Bowel 16 Channel Catheter
• 00678467508270 - Mui Scientific: 2025-06-19 Esophageal Aspiration 9 Channel Catheter
• 00678467508287 - Mui Scientific: 2025-06-19 Esophageal Aspiration 11 Channel Catheter
• 10678467000559 - Mui Scientific: 2025-05-19 Single Use Esophageal 4 Channel Catheter
• 00678467508263 - Mui Scientific: 2025-04-23 Esophageal 4 Channel Catheter
• 00678467508256 - Mui Scientific: 2025-04-23 Single Use Anorectal 8 Channel Catheter
• 00678467508232 - Mui Scientific: 2025-04-18 Single Use Anorectal 16 Ch Catheter