Identity
- Trade Name
- HeartMate 3™ FDA UDI
- Generic Name
- Skin-coring punch, single-use FDA UDI
- Device Name
- Skin Coring Punch FDA UDI
- Model / Reference
- 106528US FDA UDI
- Description
- Skin Coring Punch FDA UDI
Identifiers
- Catalog Number
- 106528US FDA UDI
- Primary DI / UDI-DI
- 05415067039361 FDA UDI
- PMA Number
- P160054 FDA UDI
- FDA Product Code
- DSQ FDA UDI
- GMDN Term
- Skin-coring punch, single-use 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
No
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
No
FDA UDI
Category: Skin-coring punch, single-use
HeartMate 3™ by Thoratec Corp — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin-coring punch, single-use.
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- EDM3 — EDM 3, LLC · Class I
- SHARD — APPLIED DENTAL, INC. · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- EDM3 — EDM 3, LLC · Class I
- MedSource Skin Biopsy Punch — MEDSOURCE INTERNATIONAL LLC · Class I
- Biopsy Punches, Sterile, Mixed Box — Dynarex Corp. · Class I
Cleared under the same submission
P160054 also covers:
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
- HeartMate 3™ — Thoratec Corp
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Thoratec Corp
Sources (1)
- FDA UDI 1fb907d6-0aa1-4159-8280-09960f57c2aa 37 fields · synced Jun 7, 2026