Primary Device ID | 16928081771293 |
NIH Device Record Key | 4be803d6-fdf9-4273-92eb-0cf2fe79208a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | arboleaf |
Version Model Number | CS20W |
Company DUNS | 421347580 |
Company Name | Shenzhen Yolanda Technology Co.,Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Serial Number | false |
Manufacturing Date | false |
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 | 06928081771296 [Primary] |
GS1 | 16928081771293 [Package] Contains: 06928081771296 Package: [6 Units] In Commercial Distribution |
PUH | Analyzer, Body Composition, Exempt |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-10-24 |
Device Publish Date | 2023-10-16 |
16928081771293 | CS20W |
16928081771255 | SP10A |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ARBOLEAF 97890256 not registered Live/Pending |
ARBOLEAF CORPORATION 2023-04-15 |
![]() ARBOLEAF 90664956 not registered Live/Pending |
Arboleaf Corporation 2021-04-22 |
![]() ARBOLEAF 88642974 not registered Live/Pending |
Arboleaf Corporation 2019-10-04 |
![]() ARBOLEAF 87873312 5651617 Live/Registered |
ARBOLEAF CORPORATION 2018-04-11 |