Bentley Manual Tilt Wheelchair 5510

GUDID B829101

PDG Product Design Group Inc

Wheelchair, attendant/occupant-driven, rear-wheels-operated, non-collapsible
Primary Device IDB829101
NIH Device Record Key7b7c5de0-5f59-4a31-baf5-c37e614a6966
Commercial Distribution StatusIn Commercial Distribution
Brand NameBentley Manual Tilt Wheelchair
Version Model NumberBENTLEY
Catalog Number5510
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
HIBCCB829101 [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 [Bentley Manual Tilt Wheelchair]

B829241BENTLEY LT
B829101BENTLEY
B829271BENTLEY LT-R

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.