Primary Device ID | 06946725520499 |
NIH Device Record Key | a4d353df-6423-473c-83ce-bc5f5e91aac6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HP |
Version Model Number | A0816-SA106PU |
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 | 06946725520499 [Primary] |
GS1 | 16946725597948 [Package] Package: [25 Units] In Commercial Distribution |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-03-06 |
06946725520529 | A0816-SW106PU |
06946725520512 | A0816-SP106PU |
06946725520505 | A0816-SP106PV |
06946725520499 | A0816-SA106PU |
06946725520482 | A0816-SA106PV |
06946725520468 | A0816-SW105PU |
06946725520451 | A0816-SP105PU |
06946725520444 | A0816-SP105PV |
06946725520437 | A0816-SA105PU |
06946725520420 | A0816-SA105PV |