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 |