Solo RepoSheet™ lift aid

GUDID 00887761976757

Patient lifting system stretcher

Liko AB

Patient lifting system stretcher Patient lifting system stretcher Patient lifting system stretcher Patient lifting system stretcher Patient lifting system stretcher Patient lifting system stretcher Patient lifting system stretcher
Primary Device ID00887761976757
NIH Device Record Keye900944e-4f0d-4190-915d-de9eef8d4d4b
Commercial Distribution StatusIn Commercial Distribution
Brand NameSolo RepoSheet™ lift aid
Version Model Number36871004
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100887761976757 [Package]
Contains: 00887761984295
Package: [8 Units]
In Commercial Distribution
GS100887761984295 [Primary]

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 Date2021-08-09
Device Publish Date2021-07-31

On-Brand Devices [Solo RepoSheet™ lift aid]

10887761984278Patient lifting system stretcher
00887761976757Patient lifting system stretcher

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