Primary Device ID | 00860003056639 |
NIH Device Record Key | f5042588-7ad8-46eb-926f-f9ace8fabb1f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RoughRider |
Version Model Number | Aurora |
Company DUNS | 052942916 |
Company Name | Roughrider America LLC |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860003056639 [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 | 2023-03-09 |
Device Publish Date | 2023-03-01 |
00860009406087 | manually propelled wheelchair |
00860009406070 | manually propelled wheelchair |
00860009406063 | manually propelled wheelchair |
00860009406056 | manually propelled wheelchair |
00860009406049 | manually propelled wheelchair |
00860009406032 | manually propelled wheelchair |
00860009406025 | manually propelled wheelchair |
00860009406018 | manually propelled wheelchair |
00860009406001 | manually propelled wheelchair |
00860003056677 | Manually Propelled Wheelchair |
00860003056660 | Manually Propelled Wheelchair |
00860003056653 | Manually Propelled Wheelchair |
00860003056646 | Manually Propelled Wheelchair |
00860003056639 | Manually Propelled Wheelchair |
00860003056622 | Manually Propelled Wheelchair |
00860003056615 | Manually Propelled Wheelchair |
00860003056608 | Manually Propelled Wheelchair |