Primary Device ID | 06958481454444 |
NIH Device Record Key | 9e57f53a-f312-46d0-b59d-5869c25f4dfa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Apollo Balloon Dilatation Catheter |
Version Model Number | rev 02 |
Catalog Number | 802-4025U |
Company DUNS | 421318800 |
Company Name | BrosMed Medical 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 | false |
OTC Over-The-Counter | false |