eudamed_udi
Primary ID: H671CUR1000
Endocurette (UDI H671CUR1000)
Manufactured by Utah Medical Products, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Endocurette - Primary ID H671CUR1000
Device Regulatory Overview
The Endocurette (Model/Catalog Number: CUR-100) is a medical device manufactured by Utah Medical Products, Inc.. This product is indexed under FDA Product Code / Category Classification U080101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CUR-100
- Product Code / EMDN
- U080101
- Device Name
- Endocurette
- Database Sync Date
- 2026-08-09 16:29:17
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Endocurette?
The registered manufacturer of record for Endocurette is Utah Medical Products, Inc..
What is the Primary UDI-DI identifier for Endocurette?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is H671CUR1000.
What classification code is assigned to this device?
This device is registered under product classification code U080101.
Similar Classification Devices (U080101)
Other Devices by Utah Medical Products, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint