Primary Device ID | 06974368460032 |
NIH Device Record Key | 6ba4941d-de3c-4773-b35a-11d7f87b0787 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Achepower |
Version Model Number | AR-W-06C |
Company DUNS | 700105391 |
Company Name | Shenzhen Achepower Electronic 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 | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 06974368460032 [Primary] |
EFS | Unit, Oral Irrigation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-02-17 |
Device Publish Date | 2023-02-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACHEPOWER 88727272 not registered Live/Pending |
Shenzhen YJK Technology Co., Ltd 2019-12-13 |