CONDUIT 174A
HANCOCK® - 174A-20
Device Description
An implantable artificial substitute for a blood vessel intended to replace or bypass a diseased or injured vessel, typically the aorta, an iliac, a femoral or popliteal artery; it is not intended for use in the coronary arteries. It is typically made of woven or knitted polyethylene terephthalate (Dacron) or polytetrafluoroethylene (PTFE) fabrics; it does not incorporate a metallic mesh (i.e., it is not a stent-graft).
Environmental Conditions
No Data Available
Device Sizes
- Valve Size 20 MM
Device Sterilization
Device Sterile: False
Sterilization Prior To Use: True
Sterilization Methods:
- Moist Heat or Steam Sterilization
Product Codes
Code: DYE
Device Name: Replacement Heart-Valve
Device Class: 3
Physical State: N/A
Definition: Call for pmas to be filed by 12/9/87 (52 fr 23137 (6/17/87))
Submission Type ID: 2
Review Panel: CV
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: Y
Target Area: N/A
Regulation Number: 870.3925
Third Party Flag: N
Medical Specialty: CV
Device IdentifiersDevice Id: 00613994578686
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A