Primary Device ID | 06946725526040 |
NIH Device Record Key | 943ae7e1-af38-428c-bd91-7d07008f4f5a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Datascope |
Version Model Number | A0405-SP203PV |
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 | 06946725526040 [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 |
06946725526064 | A0405-SW203PU |
06946725526057 | A0405-SP203PU |
06946725526040 | A0405-SP203PV |
06946725526033 | A0405-SA203PU |
06946725526026 | A0405-SA203PV |
06946725526019 | A0405-SW115PU |
06946725526002 | A0405-SP115PU |
06946725525999 | A0405-SP115PV |
06946725525982 | A0405-SA115PU |
06946725525975 | A0405-SA115PV |