Primary Device ID | 08809471725977 |
NIH Device Record Key | 391e4a0d-fe79-49f1-a76a-8d72f4b7acd7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multi Gauge |
Version Model Number | KDGP13 |
Company DUNS | 688753763 |
Company Name | Cowellmedi 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 | false |
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 |