E-Yoke Regulator O2 35013

GUDID 00813830022377

ACCUTRON, INC.

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• Primary Device ID: 00813830022377
• NIH Device Record Key: 527d0d4c-6ff0-46cf-9cd4-a1796ee56b51
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E-Yoke Regulator O2
• Version Model Number: 35013
• Catalog Number: 35013
• Company DUNS: 088302096
• Company Name: ACCUTRON, 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813830022377 [Primary]

FDA Product Code

• CAM: Yoke Assembly, Medical Gas

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-26

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