TransMatt TM34DIS

GUDID 00816299011036

34" TransMatt Decedent Transfer System

Hovertech International

Patient transfer system, powered

• Primary Device ID: 00816299011036
• NIH Device Record Key: b0b0b092-5465-41b6-a16c-1d2f73ed3755
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TransMatt
• Version Model Number: TM34DIS
• Catalog Number: TM34DIS
• Company DUNS: 942139841
• Company Name: Hovertech International
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)471-2776
• Email: info@hovermatt.com
• Phone: +1(800)471-2776
• Email: info@hovermatt.com
• Phone: +1(800)471-2776
• Email: info@hovermatt.com

Device Dimensions

• Width: 34 Inch
• Width: 34 Inch
• Width: 34 Inch

Operating and Storage Conditions

• Storage Environment Temperature: Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816299011036 [Package]; Contains: 00816299011043; Package: box [5 Units]; In Commercial Distribution
GS1	00816299011043 [Primary]

FDA Product Code

• FRZ: DEVICE, PATIENT TRANSFER, POWERED

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: 2016-07-30

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