Liko Original HighBack Sling™, Mod. 210

GUDID 00887761983281

Patient lifting system divided leg sling

Liko AB

Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling Patient lifting system divided leg sling
Primary Device ID00887761983281
NIH Device Record Key0197226e-20e8-4199-92c7-ffd8b6e7fcc3
Commercial Distribution StatusIn Commercial Distribution
Brand NameLiko Original HighBack Sling™, Mod. 210
Version Model Number35210115
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
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [Primary]
GS100887761983281 [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 Date2020-06-23
Device Publish Date2020-06-15

On-Brand Devices [Liko Original HighBack Sling™, Mod. 210]

00887761983335Patient lifting system divided leg sling
00887761983328Patient lifting system divided leg sling
00887761983304Patient lifting system divided leg sling
00887761983281Patient lifting system divided leg sling
00887761983274Patient lifting system divided leg sling

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