Primary Device ID | 06971591762476 |
NIH Device Record Key | 7d3bc7bb-9e61-48d6-b844-798b37d51f05 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Selethru PTCA Balloon Dilatation Catheter |
Version Model Number | KPTCA300010 |
Company DUNS | 560219894 |
Company Name | Kossel Medtech (Suzhou) 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 | 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 |