Identity
- Trade Name
- Acessa ProVu System FDA UDI
- Generic Name
- Electromagnetic device tracking/ultrasound guided radio-frequency ablation system console/generator FDA UDI
- Device Name
- The Acessa ProVu Console Dual Foot Pedal FDA UDI
- Model / Reference
- MS-06-0171 FDA UDI
- Description
- The Acessa ProVu Console Dual Foot Pedal FDA UDI
Identifiers
- Catalog Number
- MS-06-0171 FDA UDI
- Primary DI / UDI-DI
- 15420045515314 FDA UDI
- FDA Product Code
- HFG FDA UDI
- GMDN Term
- Electromagnetic device tracking/ultrasound guided radio-frequency ablation system console/generator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.4160 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electromagnetic device tracking/ultrasound guided radio-frequency ablation system console/generator
Acessa ProVu System by Hologic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electromagnetic device tracking/ultrasound guided radio-frequency ablation system console/generator.
- Acessa ProVu System — Hologic, Inc. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Hologic, Inc.
Sources (1)
- FDA UDI dc1f45d2-af55-4c6b-b5b3-abf9c0000441 36 fields · synced May 30, 2026