RIK VL22000E

GUDID 05055982799324

RIK Fluid Overlay

Arjohuntleigh AB

Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay Foam-filled bed mattress overlay
Primary Device ID05055982799324
NIH Device Record Key4d31c361-5d7d-4d04-b12f-7220b4956eb9
Commercial Distribution StatusIn Commercial Distribution
Brand NameRIK
Version Model NumberVL22000E
Catalog NumberVL22000E
Company DUNS355804758
Company NameArjohuntleigh 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 Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com
Phone+1(800) 323-1245
Emailus.info@arjo.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105055982799324 [Primary]

FDA Product Code

IKYMattress, Flotation Therapy, Non-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-07
Device Publish Date2023-07-30

On-Brand Devices [RIK]

05055982799324RIK Fluid Overlay
05055982799317RIK Fluid Overlay
05055982799300RIK 400 Fluid Operating Table Pad
05055982799294RIK 300 Fluid Operating Table Pad

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