Identity
- Trade Name
- Genesys HTA Control Unit FDA UDI
- Generic Name
- Circulating-fluid endometrial-ablation control unit FDA UDI
- Device Name
- Genesys HTA 115V Control Unit FDA UDI
- Model / Reference
- M006580010 FDA UDI
- Description
- Genesys HTA 115V Control Unit FDA UDI
Identifiers
- Catalog Number
- M006580010 FDA UDI
- Primary DI / UDI-DI
- 00850033976014 FDA UDI
- FDA Product Code
- MNB FDA UDI
- GMDN Term
- Circulating-fluid endometrial-ablation control unit FDA UDI
Classification
- Device Class
- Class III 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
Yes
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
Yes
FDA UDI
Category: Circulating-fluid endometrial-ablation control unit
Genesys HTA Control Unit by Minerva Surgical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Circulating-fluid endometrial-ablation control unit.
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- Genesys HTA Control Unit - Refurbished — MINERVA SURGICAL, INC. · 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
- Minerva Surgical, Inc.
Sources (1)
- FDA UDI 5c370c16-9acd-406a-804a-af458606faa0 35 fields · synced May 30, 2026