Primary Device ID | 06946725525906 |
NIH Device Record Key | 798deaa2-481b-427f-8845-d2a7ef6f12e1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CSI |
Version Model Number | A0309-SP202PU |
Company DUNS | 529691989 |
Company Name | APK Technology Co.,Ltd. |
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 | true |
Manufacturing Date | false |
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 | 06946725525906 [Primary] |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-04-10 |
06946725525913 | A0309-SW202PU |
06946725525906 | A0309-SP202PU |
06946725525890 | A0309-SP202PV |
06946725525883 | A0309-SA202PU |
06946725525876 | A0309-SA202PV |
06946725525869 | A0309-SW111PU |
06946725525852 | A0309-SP111PU |
06946725525845 | A0309-SP111PV |
06946725525838 | A0309-SA111PU |
06946725525821 | A0309-SA111PV |
06946725525814 | A0309-SW102PU |
06946725525807 | A0309-SP102PU |
06946725525791 | A0309-SP102PV |
06946725525784 | A0309-SA102PU |
06946725525777 | A0309-SA102PV |