Liko SilhouetteSling™, Mod. 22

GUDID 00887761983359

Patient lifting system divided leg sling

Liko AB

Patient lifting system divided leg sling

• Primary Device ID: 00887761983359
• NIH Device Record Key: 9aae6b77-7dd2-451a-b845-dbe5d5744323
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Liko SilhouetteSling™, Mod. 22
• Version Model Number: 3522603
• 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: true
• 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

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
• 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
• 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	00887761983359 [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: 2020-06-30
• Device Publish Date: 2020-06-22

On-Brand Devices [Liko SilhouetteSling™, Mod. 22]

• 00887761983373: Patient lifting system divided leg sling
• 00887761983366: Patient lifting system divided leg sling
• 00887761983342: Patient lifting system divided leg sling
• 00887761983359: Patient lifting system divided leg sling