Identity
- Trade Name
- Genesys HTA ProCerva FDA UDI
- Generic Name
- Circulating-fluid endometrial-ablation catheter FDA UDI
- Device Name
- Procedure Set including Procedure Sheath, Cassette, Drainage Bag FDA UDI
- Model / Reference
- M006580210 FDA UDI
- Description
- Procedure Set including Procedure Sheath, Cassette, Drainage Bag FDA UDI
Identifiers
- Catalog Number
- M006580210 FDA UDI
- Primary DI / UDI-DI
- 00850033976038 FDA UDI
- FDA Product Code
- MNB FDA UDI
- GMDN Term
- Circulating-fluid endometrial-ablation catheter 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: Circulating-fluid endometrial-ablation catheter
Genesys HTA ProCerva by Minerva Surgical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 a289ace3-e8e8-4813-87c2-d92737c9ef52 35 fields · synced Jun 8, 2026