Primary Device ID | 06976025820012 |
NIH Device Record Key | 4d021162-604f-4f00-b167-973856ef370c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hupai |
Version Model Number | 3ml 0.7×30mm |
Company DUNS | 713864194 |
Company Name | Jiangsu Chongheng Medical Technology Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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 | 06976025820012 [Primary] |
CBT | Arterial Blood Sampling Kit |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-16 |
Device Publish Date | 2023-03-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() HUPAI 90319500 not registered Live/Pending |
Luo, Jintao 2020-11-14 |