Liko UniversalSling™, Mod. 000

GUDID 00887761982628

Patient lifting system divided leg sling

Liko AB

Patient lifting system divided leg sling

• Primary Device ID: 00887761982628
• NIH Device Record Key: e08f73ea-8cb1-43b2-a19d-26721ca6e739
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Liko UniversalSling™, Mod. 000
• Version Model Number: 35000111
• 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: 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
• 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	00887761982628 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-04-07
• Device Publish Date: 2020-06-11

On-Brand Devices [Liko UniversalSling™, Mod. 000]

• 00887761982666: Patient lifting system divided leg sling
• 00887761982895: Patient lifting system divided leg sling
• 00887761982888: Patient lifting system divided leg sling
• 00887761982871: Patient lifting system divided leg sling
• 00887761982864: Patient lifting system divided leg sling
• 00887761982857: Patient lifting system divided leg sling
• 00887761982840: Patient lifting system divided leg sling
• 00887761982833: Patient lifting system divided leg sling
• 00887761982826: Patient lifting system divided leg sling
• 00887761982819: Patient lifting system divided leg sling
• 00887761982802: Patient lifting system divided leg sling
• 00887761982796: Patient lifting system divided leg sling
• 00887761982789: Patient lifting system divided leg sling
• 00887761982772: Patient lifting system divided leg sling
• 00887761982765: Patient lifting system divided leg sling
• 00887761982758: Patient lifting system divided leg sling
• 00887761982741: Patient lifting system divided leg sling
• 00887761982734: Patient lifting system divided leg sling
• 00887761982727: Patient lifting system divided leg sling
• 00887761982710: Patient lifting system divided leg sling
• 00887761982703: Patient lifting system divided leg sling
• 00887761982697: Patient lifting system divided leg sling
• 00887761982680: Patient lifting system divided leg sling
• 00887761982673: Patient lifting system divided leg sling
• 00887761982659: Patient lifting system divided leg sling
• 00887761982642: Patient lifting system divided leg sling
• 00887761982635: Patient lifting system divided leg sling
• 00887761982628: Patient lifting system divided leg sling