Medium Tricycle

GUDID 00858101008537

Adaptive Tricycle

RIFTON EQUIPMENT

Assistive foot-propelled tricycle
Primary Device ID00858101008537
NIH Device Record Key9573dd4f-2dbf-4088-8208-6641b335f42e
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedium Tricycle
Version Model NumberR130
Company DUNS808251438
Company NameRIFTON EQUIPMENT
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

Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com
Phone800.571.8198
EmailSales@rifton.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100858101008537 [Primary]

FDA Product Code

IONExerciser, Non-Measuring

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-21
Device Publish Date2022-09-13

On-Brand Devices [Medium Tricycle]

00858101008537Adaptive Tricycle
00850001752312Adaptive Tricycle

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