FLOWMETER. THORPE

GUDID 00628101609764

FM-T series, 200 CC, USA, 50PSI, CO2

OHIO MEDICAL, LLC

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• Primary Device ID: 00628101609764
• NIH Device Record Key: 2d28a4fa-6cd2-4e04-858c-f92f81d1b4ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FLOWMETER. THORPE
• Version Model Number: FM-OT-2CUC
• Company DUNS: 005192885
• Company Name: OHIO MEDICAL, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM
• Phone: 1 847 855 0500
• Email: CUSTOMER.SERVICE@OHIOMEDICAL.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00628101609764 [Primary]

FDA Product Code

• CAX: Flowmeter, Tube, Thorpe, Back-Pressure Compensated

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: 2020-09-14
• Device Publish Date: 2020-09-04

Devices Manufactured by OHIO MEDICAL, LLC

• 00628101621544 - Ohio: 2023-08-09 GR 60 PSI PRESET ISO AIR REG CGA 346 DC
• 00628101621575 - Ohio: 2023-08-09 60 PSI PRESET COMPACT CO2 REG CGA 320 ISO
• 00628101621582 - Ohio: 2023-08-09 GAS REGULATOR CGA 326 N2O DC*DC
• 00628101621599 - Ohio: 2023-08-09 50 PSI PRST REG CGA 346 AIR IN BF OUT
• 00628101621605 - Ohio: 2023-08-09 50 PSI PRST REG CGA 346 AIR IN CO CH OUT
• 00628101621612 - Ohio: 2023-08-09 50 PSI PRST REG CGA 346 AIR IN pF OUT
• 00628101621629 - Ohio: 2023-08-09 GAS REG 50 PSI PRST CGA 540 INLET BF OUT
• 00628101621636 - Ohio: 2023-08-09 50 PSI PRST OXY REG CGA 540 IN CO CH OUT