gudid
Primary ID: URR-ICP
V. Mueller (UDI URR-ICP)
Manufactured by STERIS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for V. Mueller - Primary ID URR-ICP
Device Regulatory Overview
The V. Mueller (Model/Catalog Number: URR-ICP) is a medical device manufactured by STERIS CORPORATION. This product is indexed under FDA Product Code / Category Classification KCT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- URR-ICP
- Product Code / EMDN
- KCT
- Device Name
- UNIVERSAL RING RETRACTION SET CLAMPS AND POSTS INSERT
- Database Sync Date
- 2026-08-09 09:16:32
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 V. Mueller?
The registered manufacturer of record for V. Mueller is STERIS CORPORATION.
What is the Primary UDI-DI identifier for V. Mueller?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is URR-ICP.
What classification code is assigned to this device?
This device is registered under product classification code KCT.
Similar Classification Devices (KCT)
Other Devices by STERIS CORPORATION
Programmatic Export
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