Primary Device ID | 06953775661263 |
NIH Device Record Key | 530e64ce-5e29-41b8-8c6f-335bcfcd0963 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AILIFEE |
Version Model Number | AES-U632 |
Company DUNS | 548040741 |
Company Name | Alicn Medical Shenzhen, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 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 | 06953775661263 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-27 |
Device Publish Date | 2025-05-19 |
06953775661263 | AES-U632 |
06953775661256 | AES-U612 |
06953775661249 | AET-R1F1 |
06953775661232 | AES-U392 |
06953775661225 | AES-U231 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() AILIFEE 87944091 5649055 Live/Registered |
ALICN MEDICAL SHENZHEN INC 2018-05-31 |