Flotec

GUDID B741HA0

FLOTEC INC

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• Primary Device ID: B741HA0
• NIH Device Record Key: b41e8e2d-a50e-46b5-8342-8a7d596ada56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flotec
• Version Model Number: Hose Assembly
• Company DUNS: 103643730
• Company Name: FLOTEC INC
• 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: true
• Serial Number: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B741HA0 [Primary]

FDA Product Code

• BYX: Tubing, Pressure And Accessories

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: 2021-10-15
• Device Publish Date: 2021-10-07

On-Brand Devices [Flotec]

• B741RW0: RW Regulator
• B741MC0: Mass Casualty Assembly
• B741FM0: Flowmeter
• B741DL0: InGage Regulator
• B741HA0: Hose Assembly
• B741CH0: Hose Assembly - Canadian Standard
• B741TCB0: T.O.A.D. Connection Box