Liko SilhouetteSling™, Mod. 22

GUDID 00887761983373

Patient lifting system divided leg sling

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, battery-powered
Primary Device ID00887761983373
NIH Device Record Key51388225-e599-4135-89e3-46180e943ee6
Commercial Distribution StatusIn Commercial Distribution
Brand NameLiko SilhouetteSling™, Mod. 22
Version Model Number3522605
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 Datefalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]
GS100887761983373 [Primary]

FDA Product Code

FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered
FSALift, patient, non-ac-powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-17
Device Publish Date2020-06-09

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

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

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