Identity
- Trade Name
- Mencini FDA UDI
- Generic Name
- Intrauterine imaging medium catheter FDA UDI
- Device Name
- Mencini Double Balloon Hysterosalpingography Catheter FDA UDI
- Model / Reference
- G10432 FDA UDI
- Description
- Mencini Double Balloon Hysterosalpingography Catheter FDA UDI
Identifiers
- Catalog Number
- DBH-100 FDA UDI
- Primary DI / UDI-DI
- 00827002104327 FDA UDI
- FDA Product Code
- HES FDA UDI
- GMDN Term
- Intrauterine imaging medium catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1300 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
Yes
FDA UDI
Category: Intrauterine imaging medium catheter
Mencini by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intrauterine imaging medium catheter.
- Rocket — Rocket Medical Plc
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- Rocket — Rocket Medical Plc · Class II
- Batrik H/S Catheter TM 5F — Batrik Medical Manufacturing Inc · Class II
- Rocket — Rocket Medical Plc
- Hysterosalpingography (HSG) Catheter — Argon Medical Devices, Inc. · Class II
- Bioteque Taiwan Ltd. — Bioteque Taiwan Ltd. · Class II
- TVUS/HSG-Cath — Utah Medical Products, 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
- Cook Incorporated
Sources (1)
- FDA UDI 2c108320-a2b1-42fc-8a76-ebf0455cea58 36 fields · synced Jun 8, 2026