Fuze Manual Tilt Wheelchair 5515

GUDID B829151

PDG Product Design Group Inc

Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible
Primary Device IDB829151
NIH Device Record Key18a05211-6668-4d17-96d4-900c1733323f
Commercial Distribution StatusIn Commercial Distribution
Brand NameFuze Manual Tilt Wheelchair
Version Model NumberFUZE T50
Catalog Number5515
Company DUNS253873905
Company NamePDG Product Design Group Inc
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
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

Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com
Phone888-858-4422
Emailinfo@pdgmobility.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB829151 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IORWheelchair, Mechanical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-06
Device Publish Date2020-09-28

On-Brand Devices [Fuze Manual Tilt Wheelchair]

B829261FUZE T50N
B829171FUZE JR
B829161FUZE T20
B829151FUZE T50
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