Titan Stretcher

GUDID 00807251000014

Amico Beds Corporation

Hospital stretcher, manual

• Primary Device ID: 00807251000014
• NIH Device Record Key: 50c4681d-8bcc-48d5-b75f-2e7c1a4fb164
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Titan Stretcher
• Version Model Number: S-AM1-300X
• Company DUNS: 202806964
• Company Name: Amico Beds Corporation
• 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: true
• Manufacturing Date: true
• 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	00807251000014 [Primary]

FDA Product Code

• FPO: Stretcher, Wheeled

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: 2016-07-28

Devices Manufactured by Amico Beds Corporation

• 00807251000007 - Titan S-H-300 Stretcher: 2018-03-29
• 00807251000014 - Titan Stretcher: 2018-03-29
• 00807251000014 - Titan Stretcher: 2018-03-29
• 00807251000021 - Apollo MS Electric Bed: 2018-03-29