Small Tricycle

GUDID 00850001752329

Adaptive Tricycle

RIFTON EQUIPMENT

Assistive foot-propelled tricycle
Primary Device ID00850001752329
NIH Device Record Key7101f7c6-7ee0-42d4-b762-eff1dfa38c75
Commercial Distribution StatusIn Commercial Distribution
Brand NameSmall Tricycle
Version Model NumberX320
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
GS100850001752329 [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 Date2023-06-23
Device Publish Date2023-06-15

On-Brand Devices [Small Tricycle]

00858101008513Adaptive Tricycle
00850001752329Adaptive Tricycle

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.