Primary Device ID | 00146191201908 |
NIH Device Record Key | 5cee4e75-85ee-4d3a-be81-85ea1106eb11 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Andesfit |
Version Model Number | ADF-B19 |
Company DUNS | 664101036 |
Company Name | ANDESFIT LIMITED |
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 | true |
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 | 00146191201908 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2019-03-15 |
00146191200604 | Wireless Pules Oximeter |
00146191210221 | Wireless Wrist Type Blood Pressure Monitor |
00146191201908 | Wireless Arm Type Blood Pressure monitor |
00146191010005 | Wireless Spirometer |
00146191203803 | Wireless Non-Contact Infrared Body/Surface Thermometer |
04897100310254 | Upper Arm Electronic Blood Pressure Monitor |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ANDESFIT 97820912 not registered Live/Pending |
Andesfit System Limited 2023-03-02 |
![]() ANDESFIT 97820907 not registered Live/Pending |
Andesfit System Limited 2023-03-02 |