Primary Device ID | 06936534325026 |
NIH Device Record Key | 93550e46-c98b-474e-b648-5b7a8eb5ea00 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single Use Urinary Guidewire |
Version Model Number | MD-C2-UW2520 |
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 |