| Primary Device ID | 00860012388400 |
| NIH Device Record Key | c69f3e23-8f2d-4df7-8cf2-a36ed3443e15 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | culver mobility |
| Version Model Number | artemis |
| Catalog Number | 20240101 |
| Company DUNS | 080507019 |
| Company Name | CULVER LED LIGHTING SOLUTION CORP |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| 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 | 00860012388400 [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 | 2024-07-26 |
| Device Publish Date | 2024-07-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CULVER MOBILITY 98754509 not registered Live/Pending |
Culver Led Lighting Corp. 2024-09-17 |
![]() CULVER MOBILITY 97530725 not registered Live/Pending |
Culver Led Lighting Corp. 2022-08-02 |