Primary Device ID | 06970742221411 |
NIH Device Record Key | d252c69a-86bd-4738-bd44-2118a9fc5024 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DR-HO'S |
Version Model Number | CP-I |
Company DUNS | 530683813 |
Company Name | Guangzhou Xinbo Electronic 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 | false |
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 |