DynaRide S 2 Wheelchair-18"x16" Seat w/ Detach Full Arm FR

GUDID 00616784022413

DYNAREX CORPORATION

Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible
Primary Device ID00616784022413
NIH Device Record Key77054c65-3bd3-4f4d-9312-8d8184e8bf70
Commercial Distribution StatusIn Commercial Distribution
Brand NameDynaRide S 2 Wheelchair-18"x16" Seat w/ Detach Full Arm FR
Version Model Number10224
Company DUNS008124539
Company NameDYNAREX CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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 Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100616784022413 [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 Date2019-07-02
Device Publish Date2019-06-24

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