Ohmega R

GUDID 08717775955016

Medical Measurement Systems B.V.

Oesophageal motility analysis system

• Primary Device ID: 08717775955016
• NIH Device Record Key: 5fd134a6-8c54-40d5-b455-cfb1a06142a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ohmega R
• Version Model Number: G2-1
• Company DUNS: 416277333
• Company Name: Medical Measurement Systems B.V.
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08717775955016 [Primary]

FDA Product Code

• FFX: SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2025-06-02
• Device Publish Date: 2016-09-23

Devices Manufactured by Medical Measurement Systems B.V.

• 08717775955016 - Ohmega R: 2025-06-02
• 08717775955016 - Ohmega R: 2025-06-02
• 28717775956611 - MPP-Plus: 2025-03-03
• 08720648846083 - Flowsensor3-BT: 2024-09-25
• 08717775954828 - Flowmaster NS: 2024-07-11
• 18717775955556 - Flowstar NS: 2024-06-03
• 00814247021229 - Flowstar: 2024-04-29
• 08717775955702 - HEM: 2022-11-28
• 08717775955870 - HEM FS: 2022-11-28