Identity
- Trade Name
- Hancock™ FDA UDI
- Generic Name
- Pulmonary open-surgery heart valve bioprosthesis FDA UDI
- Device Name
- CONDUIT HC150-20 HK1 MO 26L FDA UDI
- Model / Reference
- HC150-20 FDA UDI
- Description
- CONDUIT HC150-20 HK1 MO 26L FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000517823 FDA UDI
- PMA Number
- P790007 FDA UDI
- FDA Product Code
- LWR FDA UDI
- GMDN Term
- Pulmonary open-surgery heart valve bioprosthesis FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Pulmonary open-surgery heart valve bioprosthesis
Hancock™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pulmonary open-surgery heart valve bioprosthesis.
- Contegra® — MEDTRONIC, INC. · Unclassified
- Contegra® — MEDTRONIC, INC. · Unclassified
- Hancock™ — MEDTRONIC, INC. · Class III
- Hancock™ 150 — MEDTRONIC, INC. · Class III
- Hancock™ — MEDTRONIC, INC. · Class III
- HANCOCK® — MEDTRONIC, INC. · Class III
- Contegra® — MEDTRONIC, INC. · Unclassified
- Hancock™ — MEDTRONIC, INC. · Class III
Cleared under the same submission
P790007 also covers:
- HANCOCK® — MEDTRONIC, INC.
- HANCOCK® — MEDTRONIC, INC.
- HANCOCK® — MEDTRONIC, INC.
- HANCOCK® — MEDTRONIC, INC.
- HANCOCK® — MEDTRONIC, INC.
- HANCOCK® — MEDTRONIC, INC.
- HANCOCK® — MEDTRONIC, INC.
- Hancock™ — MEDTRONIC, INC.
- Hancock™ — MEDTRONIC, INC.
- Hancock™ — MEDTRONIC, INC.
- Hancock™ — MEDTRONIC, INC.
- Hancock™ — MEDTRONIC, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI c97525ca-5576-45cb-86ba-9d6b9a4d0207 37 fields · synced May 30, 2026