Primary Device ID | 04570072300033 |
NIH Device Record Key | a47bedc5-1ad8-4566-8e82-993c86afe35f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WHILL, Inc. |
Version Model Number | Model C2 |
Catalog Number | 32-00022-J-02-2024-02-15 |
Company DUNS | 691746455 |
Company Name | WHILL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04570072300033 [Primary] |
ITI | Wheelchair, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-10 |
Device Publish Date | 2024-09-02 |
04570072301832 | The intended use of the WHILL Model F powered wheelchair is to provide outdoor and indoor mobili |
04570072300033 | The intended use of the WHILL Model C2 powered wheelchair is to provide outdoor and indoor mobil |
04570072300026 | The intended use of the WHILL Model C2 powered wheelchair is to provide outdoor and indoor mobil |