FixStrap™

GUDID 10887761983455

General-purpose patient lifting system sling/harness

Liko AB

General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness
Primary Device ID10887761983455
NIH Device Record Keyd1a113ba-f271-4493-9511-4eaa4e27078f
Commercial Distribution StatusIn Commercial Distribution
Brand NameFixStrap™
Version Model Number3696001
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 Numberfalse
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
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
GS100887761983458 [Primary]
GS110887761983455 [Package]
Contains: 00887761983458
Package: [10 Units]
In Commercial Distribution

FDA Product Code

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 Date2021-03-29
Device Publish Date2021-03-19

On-Brand Devices [FixStrap™]

10887761983455General-purpose patient lifting system sling/harness
10887761979595Patient transfer sliding mat

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