Prevalon 700-093

GUDID 50618029980019

TrendeMATS Mobile Air Transfer System for Trendelenburg Position

SAGE PRODUCTS, LLC

Patient transfer system, manual

• Primary Device ID: 50618029980019
• NIH Device Record Key: ae0520ce-b860-49a7-a2de-693385d2669b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Prevalon
• Version Model Number: 700-093
• Catalog Number: 700-093
• Company DUNS: 054326178
• Company Name: SAGE PRODUCTS, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com
• Phone: +1(800)323-2220
• Email: customer-service-spcl@sageproducts.com

Device Dimensions

• Length: 81 Inch
• Length: 81 Inch
• Length: 81 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch
• Width: 39 Inch
• Length: 81 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00618029980014 [Primary]
GS1	50618029980019 [Package]; Contains: 00618029980014; Package: case [5 Units]; In Commercial Distribution

FDA Product Code

• FMR: DEVICE, TRANSFER, PATIENT, MANUAL

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: 2018-12-13
• Device Publish Date: 2018-11-12

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