CUVETTES DC-80 Box 100 cuvettes 0010391.000

GUDID B154O0010391CUVEACH00

Disposable cuvettes for use with the Oxicom oximeter.

WATERS MEDICAL SYSTEMS, LLC

Intracardiac oximeter Intracardiac oximeter

• Primary Device ID: B154O0010391CUVEACH00
• NIH Device Record Key: a4152b02-6e0f-4435-85ea-dcb7dac92b28
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CUVETTES DC-80 Box 100 cuvettes
• Version Model Number: CUVETTE DC-80
• Catalog Number: 0010391.000
• Company DUNS: 556957871
• Company Name: WATERS MEDICAL SYSTEMS, LLC
• 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: true
• 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

Customer Support Contacts

• Phone: 507-288-7777
• Email: info@wtrs.com
• Phone: 507-288-7777
• Email: info@wtrs.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B154O0010391CUVEACH00 [Primary]

FDA Product Code

• DQA: Oximeter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-03-21
• Device Publish Date: 2017-02-12

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• B154O0010391CUVEACH00 - CUVETTES DC-80 Box 100 cuvettes: 2019-03-21 Disposable cuvettes for use with the Oxicom oximeter.
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• B154O0034091LOW00 - CONTROL LIQUID, OXICOM - Low vial: 2019-03-21 Weekly use of liquid controls are important for calibration verification of the Oxicom. Liquid controls are available in three l