| Primary Device ID | 16928081771378 |
| NIH Device Record Key | fdd9598d-7513-4f0b-b41f-36cd56da1c07 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | arboleaf |
| Version Model Number | CS20N |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06928081771371 [Primary] |
| GS1 | 16928081771378 [Package] Contains: 06928081771371 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 | 2025-04-22 |
| Device Publish Date | 2025-04-14 |
| 16928081771293 | CS20W |
| 16928081771255 | SP10A |
| 16928081771361 | CS20M |
| 06928081772422 | SP20B |
| 16928081771378 | CS20N |
| 06928081772651 | CM20F |
| 06928081771449 | CM20C |
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 |