Primary Device ID | 06924054300043 |
NIH Device Record Key | ebf21e82-64a9-45d5-b11a-071045f0dda8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DANAVI |
Version Model Number | DHW-100 |
Company DUNS | 529404533 |
Company Name | SHANGHAI BERRY ELECTRONIC TECH CO., LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06924054300043 [Primary] |
OCH | Oximeter, Infrared, Sporting, Aviation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-11-10 |
Device Publish Date | 2020-11-03 |
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06924054300036 - Aluratek | 2021-11-10 Fingertip Pulse Oximeter |
06924054300043 - DANAVI | 2021-11-10Fingertip Pulse Oximeter |
06924054300043 - DANAVI | 2021-11-10 Fingertip Pulse Oximeter |
06924054330163 - NatureSpirit® | 2021-11-10 Fingertip Pulse Oximeter |
06924054330170 - NatureSpirit® | 2021-11-10 Fingertip Pulse Oximeter |
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