QA3 Patient Stretcher System 21117

GUDID 05051995008729

Anetic Aid USA LLC

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• Primary Device ID: 05051995008729
• NIH Device Record Key: 92813c07-9de1-4053-a2cf-9edf2df632f0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QA3 Patient Stretcher System
• Version Model Number: QA3 Treatment Stretcher
• Catalog Number: 21117
• 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	05051995008729 [Primary]

FDA Product Code

• FPO: Stretcher, Wheeled

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

On-Brand Devices [QA3 Patient Stretcher System]

• 05051995008729: QA3 Treatment Stretcher
• 05051995008712: QA3 DRIVE Powered Patient Stretcher
• 05051995004912: QA3 Ophthalmic Stretcher
• 05051995000204: QA3 Powered Emergency Stretcher
• 05051995000198: QA3 DRIVE Powered Emergency Stretcher
• 05051995000181: QA3 DRIVE Emergency Stretcher
• 05051995000167: QA3 DRIVE Powered Patient Stretcher
• 05051995000150: QA3 DRIVE Patient Stretcher
• 05051995000013: QA3 Emergency Stretcher
• 05051995000006: QA3 Patient Stretcher