Primary Device ID | 06934955979149 |
NIH Device Record Key | 7e630dbf-991a-4442-aba5-6dfa76bac55f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sapphire ULTRA Coronary Dilatation Catheter |
Version Model Number | 7917-015-11 |
Company DUNS | 530923226 |
Company Name | OrbusNeich Medical (ShenZhen) 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 | true |
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 |