Identity
- Trade Name
- Minitouch FDA UDI
- Generic Name
- Microwave ablation system probe, non-powered FDA UDI
- Device Name
- Minitouch 3.8 Era Handpiece, sterile, boxed FDA UDI
- Model / Reference
- Handpiece 3.8 Era FDA UDI
- Description
- Minitouch 3.8 Era Handpiece, sterile, boxed FDA UDI
Identifiers
- Catalog Number
- 4501 FDA UDI
- Primary DI / UDI-DI
- 10850044503015 FDA UDI
- PMA Number
- P230002 FDA UDI
- FDA Product Code
- MNB FDA UDI
- GMDN Term
- Microwave ablation system probe, non-powered 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Microwave ablation system probe, non-powered
Minitouch by Microcube, LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Microcube, LLC
Sources (1)
- FDA UDI 54887c2c-2122-4875-8d52-442de74bda51 35 fields · synced Jun 1, 2026