eudamed_udi
Primary ID: 05060758940015
eXroid Haemorrhoid Treatment Kit (UDI 05060758940015)
Manufactured by eXroid Technology Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for eXroid Haemorrhoid Treatment Kit - Primary ID 05060758940015
Device Regulatory Overview
The eXroid Haemorrhoid Treatment Kit (Model/Catalog Number: EXR105) is a medical device manufactured by eXroid Technology Ltd. This product is indexed under FDA Product Code / Category Classification Z120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EXR105
- Product Code / EMDN
- Z120601
- Device Name
- eXroid Haemorrhoid Treatment Kit
- Database Sync Date
- 2026-08-09 16:58:22
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 eXroid Haemorrhoid Treatment Kit?
The registered manufacturer of record for eXroid Haemorrhoid Treatment Kit is eXroid Technology Ltd.
What is the Primary UDI-DI identifier for eXroid Haemorrhoid Treatment Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060758940015.
What classification code is assigned to this device?
This device is registered under product classification code Z120601.
Similar Classification Devices (Z120601)
Other Devices by eXroid Technology Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint