eudamed_udi
Primary ID: +G072RC16408R0M
Guide Needle, 8FG (UDI +G072RC16408R0M)
Manufactured by Rhein Enterprises (Pvt) Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Guide Needle, 8FG - Primary ID +G072RC16408R0M
Device Regulatory Overview
The Guide Needle, 8FG (Model/Catalog Number: RC-164-08R) 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-164-08R
- Product Code / EMDN
- L031202
- Device Name
- Reusable, Stainless Steel, Non-Sterile Suction Cannula/Guide
- Database Sync Date
- 2026-08-09 17:06:01
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 Guide Needle, 8FG?
The registered manufacturer of record for Guide Needle, 8FG is Rhein Enterprises (Pvt) Ltd.
What is the Primary UDI-DI identifier for Guide Needle, 8FG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G072RC16408R0M.
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
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