Uno™ mobile lift

GUDID 00887761981775

Mobile patient lifting system, battery-powered

Liko AB

Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered
Primary Device ID00887761981775
NIH Device Record Key1d3f9ef8-d9fd-4b3f-a12c-4ac03c489ff0
Commercial Distribution StatusIn Commercial Distribution
Brand NameUno™ mobile lift
Version Model Number2010004
Company DUNS354818510
Company NameLiko AB
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com
Phone+1(800)445-3730
Emailus.customerservice@hillrom.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887761981775 [Primary]

FDA Product Code

FSALift, patient, non-ac-powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-04-07
Device Publish Date2020-06-08

Devices Manufactured by Liko AB

00887761968578 - Extension Belt2023-02-28 An extension Belt can be used to extend the lift strap for Likorall and Multirall. Also, it can be used together with Strap Grip
00887761968592 - Extension Belt2023-02-28 An extension Belt can be used to extend the lift strap for Likorall and Multirall. Also, it can be used together with Strap Grip
00887761968608 - Extension Belt2023-02-28 An extension Belt can be used to extend the lift strap for Likorall and Multirall. Also, it can be used together with Strap Grip
00887761968585 - Extension Belt2023-02-27 An extension Belt can be used to extend the lift strap for Likorall and Multirall. Also, it can be used together with Strap Grip
00887761979444 - Likorall™ overhead lift2021-09-27 Overhead track patient lifting/transfer system
00887761979468 - Likorall™ overhead lift2021-09-27 Overhead track patient lifting/transfer system
00887761979482 - Likorall™ overhead lift2021-09-27 Overhead track patient lifting/transfer system
00887761979505 - Likorall™ overhead lift2021-09-27 Overhead track patient lifting/transfer system

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.