Primary Device ID | 06936534322568 |
NIH Device Record Key | 5b3d2b26-f6ca-4172-8cb7-08c9f9f07f18 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single Use Urinary Guidewire |
Version Model Number | MD-A-UW2518 |
Company DUNS | 544434963 |
Company Name | Zhejiang Chuangxiang 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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |