VIASYS QDC CABLE GREEN 815000-031

GUDID 05707480042777

Ref. 1993

Ambu A/S

Polysomnograph

• Primary Device ID: 05707480042777
• NIH Device Record Key: 34d646b2-4f28-4ee5-be4d-07863f870319
• Commercial Distribution Discontinuation: 2019-01-07
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: VIASYS QDC CABLE GREEN
• Version Model Number: 815000-031
• Catalog Number: 815000-031
• Company DUNS: 305682023
• Company Name: Ambu A/S
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +14107686464
• Email: Purchase_orders@ambuUSA.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05707480042777 [Primary]

FDA Product Code

• LXJ: System, Optical Position/Movement Recording

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: 2019-02-07
• Device Publish Date: 2019-01-07

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