Primary Device ID | 36975033060077 |
NIH Device Record Key | 581badf1-f28f-4952-847c-fdb770fedddf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | Fast Response Kit |
Company DUNS | 544582165 |
Company Name | Shenzhen WAP-health Technology Co., Ltd. |
Device Count | 8 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
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 |