CITREX H3

GUDID 07640214642394

Flowmeter, calibration, gas

IMT Analytics AG

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• Primary Device ID: 07640214642394
• NIH Device Record Key: 125a31f1-fd7b-4ec8-892e-cafb5068cb21
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CITREX H3
• Version Model Number: 304.333.000
• Company DUNS: 480035934
• Company Name: IMT Analytics AG
• 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: true
• 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
GS1	07640214642141 [Package]; Package: [1 Units]; In Commercial Distribution
GS1	07640214642394 [Primary]

FDA Product Code

• BXY: Flowmeter, Calibration, Gas

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: 2022-11-25
• Device Publish Date: 2022-11-17

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• 07640214642394 - CITREX H3: 2022-11-25Flowmeter, calibration, gas
• 07640214642394 - CITREX H3: 2022-11-25 Flowmeter, calibration, gas
• 07640214641946 - CITREX H4: 2022-11-25 Flowmeter, calibration, gas
• 07640214642165 - CITREX H5: 2022-11-25 Flowmeter, calibration, gas