Solo RepoSheet™ lift aid

GUDID 00887761976757

Patient lifting system stretcher

Liko AB

Patient lifting system stretcher

• Primary Device ID: 00887761976757
• NIH Device Record Key: e900944e-4f0d-4190-915d-de9eef8d4d4b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Solo RepoSheet™ lift aid
• Version Model Number: 36871004
• Company DUNS: 354818510
• Company Name: Liko AB
• 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: 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

Customer Support Contacts

• Phone: +1(800)445-3730
• Email: us.customerservice@hillrom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hillrom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hillrom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hillrom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hillrom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hillrom.com
• Phone: +1(800)445-3730
• Email: us.customerservice@hillrom.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887761976757 [Package]; Contains: 00887761984295; Package: [8 Units]; In Commercial Distribution
GS1	00887761984295 [Primary]

FDA Product Code

• FSA: Lift, patient, non-ac-powered

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: 2021-08-09
• Device Publish Date: 2021-07-31

On-Brand Devices [Solo RepoSheet™ lift aid]

• 10887761984278: Patient lifting system stretcher
• 00887761976757: Patient lifting system stretcher