Identity
- Trade Name
- THORATEC® HEARMATE II®, SEALED INFLOW CONDUIT FDA UDI
- Generic Name
- Implantable ventricular circulatory assist system inflow cannula, animal-derived FDA UDI
- Model / Reference
- 104142Y FDA UDI
Identifiers
- Catalog Number
- 104142Y FDA UDI
- Primary DI / UDI-DI
- 00813024011620 FDA UDI
- FDA Product Code
- DSQ FDA UDI
- GMDN Term
- Implantable ventricular circulatory assist system inflow cannula, animal-derived 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Implantable ventricular circulatory assist system inflow cannula, animal-derived
Thoratec® Hearmate Ii®, Sealed Inflow Conduit by Thoratec Corp — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Implantable ventricular circulatory assist system inflow cannula, animal-derived.
- THORATEC® HEARTMATE II®, SEALED INFLOW CONDUIT — Thoratec Corp · Class III
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
- Thoratec Corp
Sources (1)
- FDA UDI ad21ec14-9484-43f0-bf73-6967a502971d 35 fields · synced Jun 8, 2026