Address:No.37 Chaoqian Rd.,Beijing,CN
Device Description : Inflation Device Kits is indicated for use in percutaneous coronary Intervention Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary angioplasty, PTCA; stent Implantation operation) provides the pressure inside the balloon.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : Yes
Prescription Use : Yes
Device Description : Inflation Device Kits is indicated for use in percutaneous coronary Intervention Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary angioplasty, PTCA; stent Implantation operation) provides the pressure inside the balloon.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : Yes
Prescription Use : Yes
Device Description : Inflation Device Kits is indicated for use in percutaneous coronary Intervention Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary angioplasty, PTCA; stent Implantation operation) provides the pressure inside the balloon.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : Yes
Prescription Use : Yes
Device Description : Inflation Device Kits is indicated for use in percutaneous coronary Intervention Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary angioplasty, PTCA; stent Implantation operation) provides the pressure inside the balloon.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : Yes
Prescription Use : Yes
Device Description : Inflation Device Kits is indicated for use in percutaneous coronary Intervention Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary angioplasty, PTCA; stent Implantation operation) provides the pressure inside the balloon.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : Yes
Prescription Use : Yes
Device Description : Inflation Device Kits is indicated for use in percutaneous coronary Intervention Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary angioplasty, PTCA; stent Implantation operation) provides the pressure inside the balloon.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : Yes
Prescription Use : Yes
Device Description : The ULTRASKINTM Hydrophilic Guide Wire consists of a Nitinol core wire, a plasti The ULTRASKINTM Hydrophilic Guide Wire consists of a Nitinol core wire, a plastic jacket with hydrophilic coating. The wire distal curve comes in different shapes such as straight, J angled and angled. The guide wire is radiopactitive under fluoroscopy.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : No
Prescription Use : Yes
Device Description : The ULTRASKINTM Hydrophilic Guide Wire consists of a Nitinol core wire, a plasti The ULTRASKINTM Hydrophilic Guide Wire consists of a Nitinol core wire, a plastic jacket with hydrophilic coating. The wire distal curve comes in different shapes such as straight, J angled and angled. The guide wire is radiopactitive under fluoroscopy.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : No
Prescription Use : Yes
Device Description : The ULTRASKIN Hydrophilic Guide Wire consists of a Nitinol core wire, a plastic The ULTRASKIN Hydrophilic Guide Wire consists of a Nitinol core wire, a plastic jacket with hydrophilic coating. The wire distal curve comes in different shapes such as straight, J angled and angled. The guide wire is radiopactitive under fluoroscopy.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : No
Prescription Use : Yes
Device Description : The ULTRASKIN Hydrophilic Guide Wire consists of a Nitinol core wire, a plastic The ULTRASKIN Hydrophilic Guide Wire consists of a Nitinol core wire, a plastic jacket with hydrophilic coating. The wire distal curve comes in different shapes such as straight, J angled and angled. The guide wire is radiopactitive under fluoroscopy.
Device Class : 2
Duns Number: 529853921
Premarket Exempt : No
Prescription Use : Yes