Primary Device ID | 16936733735920 |
NIH Device Record Key | ba50ff1e-e9e4-49d4-ae82-d096e9f0f171 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Angioway |
Version Model Number | LP-P-30-YNR |
Company DUNS | 529853921 |
Company Name | Lepu Medical Technology (Beijing) 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
16936733736156 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736149 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736132 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736125 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736118 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736101 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736095 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736088 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736071 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736064 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736057 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736040 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736033 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736026 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736019 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733736002 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735999 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735982 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735975 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735968 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735951 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735944 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735937 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735920 | Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment |
16936733735890 | The inflation device is applied to inflate/deflate balloon catheters and monitor pressure within |
16936733735883 | The inflation device is applied to inflate/deflate balloon catheters and monitor pressure within |