eudamed_udi
Primary ID: 05060069283238
Veneloc (UDI 05060069283238)
Manufactured by Richardson Healthcare Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Veneloc - Primary ID 05060069283238
Device Regulatory Overview
The Veneloc (Model/Catalog Number: 501000) is a medical device manufactured by Richardson Healthcare Limited. This product is indexed under FDA Product Code / Category Classification C90010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 501000
- Product Code / EMDN
- C90010301
- Device Name
- Single Use Tourniquets
- Database Sync Date
- 2026-08-09 17:17:23
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Veneloc?
The registered manufacturer of record for Veneloc is Richardson Healthcare Limited.
What is the Primary UDI-DI identifier for Veneloc?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060069283238.
What classification code is assigned to this device?
This device is registered under product classification code C90010301.
Similar Classification Devices (C90010301)
Other Devices by Richardson Healthcare Limited
Programmatic Export
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JSON API Endpoint