Primary Device ID | 16972382160249 |
NIH Device Record Key | e2ec373a-4604-4955-b7a7-fc49c10c6373 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DR. SANA |
Version Model Number | AS-302-L |
Company DUNS | 544491528 |
Company Name | XIAMEN ACURIO INSTRUMENT CO.,LTD |
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 | false |
Lot Batch | true |
Serial Number | true |
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 | 06972382160235 [Primary] |
GS1 | 16972382160249 [Package] Contains: 06972382160235 Package: [100 Units] In Commercial Distribution |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-30 |
Device Publish Date | 2020-10-22 |
16972382160256 - acurio | 2022-06-02 |
10810053630010 - SANTAMEDICAL | 2021-11-10 |
16972382160201 - SANTAMEDICAL | 2021-11-10 |
16972382160249 - DR. SANA | 2020-10-30 |
16972382160249 - DR. SANA | 2020-10-30 |
16972382160225 - acurio | 2020-07-08 |
16972382160188 - acurio | 2020-06-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DR. SANA 88866357 not registered Live/Pending |
ELIAS, NATIVIDAD 2020-04-09 |
![]() DR. SANA 77736648 4002919 Live/Registered |
Elias, Natividad R. 2009-05-14 |