QA4 Mobile Surgery System 21300

GUDID 05051995000020

Anetic Aid USA LLC

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• Primary Device ID: 05051995000020
• NIH Device Record Key: 0858d923-03fa-440b-841e-e18493f30720
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QA4 Mobile Surgery System
• Version Model Number: QA4 Mobile Surgery Platfrom
• Catalog Number: 21300
• Company DUNS: 083649158
• Company Name: Anetic Aid USA LLC
• 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: 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
GS1	05051995000020 [Primary]

FDA Product Code

• GDC: Table, Operating-Room, Electrical

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: 2023-09-19
• Device Publish Date: 2023-09-11

Devices Manufactured by Anetic Aid USA LLC

• 05051995000006 - QA3 Patient Stretcher System: 2023-09-19
• 05051995000013 - QA3 Patient Stretcher System: 2023-09-19
• 05051995000020 - QA4 Mobile Surgery System: 2023-09-19
• 05051995000020 - QA4 Mobile Surgery System: 2023-09-19
• 05051995000150 - QA3 Patient Stretcher System: 2023-09-19
• 05051995000167 - QA3 Patient Stretcher System: 2023-09-19
• 05051995000181 - QA3 Patient Stretcher System: 2023-09-19
• 05051995000198 - QA3 Patient Stretcher System: 2023-09-19
• 05051995000204 - QA3 Patient Stretcher System: 2023-09-19