eudamed_udi
Primary ID: +G072RC11240R0B
Krause Trocar 4.0mm (UDI +G072RC11240R0B)
Manufactured by Rhein Enterprises (Pvt) Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Krause Trocar 4.0mm - Primary ID +G072RC11240R0B
Device Regulatory Overview
The Krause Trocar 4.0mm (Model/Catalog Number: RC-112-40R) is a medical device manufactured by Rhein Enterprises (Pvt) Ltd. This product is indexed under FDA Product Code / Category Classification L031202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RC-112-40R
- Product Code / EMDN
- L031202
- Device Name
- Reusable, Stainless Steel, Non-Sterile Suction Cannula/Guide
- Database Sync Date
- 2026-08-09 16:49:52
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 Krause Trocar 4.0mm?
The registered manufacturer of record for Krause Trocar 4.0mm is Rhein Enterprises (Pvt) Ltd.
What is the Primary UDI-DI identifier for Krause Trocar 4.0mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G072RC11240R0B.
What classification code is assigned to this device?
This device is registered under product classification code L031202.
Similar Classification Devices (L031202)
Other Devices by Rhein Enterprises (Pvt) Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint