Primary Device ID | B829171 |
NIH Device Record Key | 1bf5d01e-f18e-426c-9705-464703480f05 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fuze Manual Tilt Wheelchair |
Version Model Number | FUZE JR |
Catalog Number | 5517 |
Company DUNS | 253873905 |
Company Name | PDG Product Design Group Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com | |
Phone | 888-858-4422 |
info@pdgmobility.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B829171 [Primary] |
IOR | Wheelchair, Mechanical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-06 |
Device Publish Date | 2020-09-28 |
B829261 | FUZE T50N |
B829171 | FUZE JR |
B829161 | FUZE T20 |
B829151 | FUZE T50 |
B829281 | FUZE M50 |