Medium Tricycle

GUDID 00850001752312

Adaptive Tricycle

RIFTON EQUIPMENT

Assistive foot-propelled tricycle
Primary Device ID00850001752312
NIH Device Record Keyd7e1d4ed-efc9-4b4a-a140-97bd69f3251a
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedium Tricycle
Version Model NumberX330
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100850001752312 [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 Date2023-05-16
Device Publish Date2023-05-08

On-Brand Devices [Medium Tricycle]

00858101008537Adaptive Tricycle
00850001752312Adaptive Tricycle

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