gudid
Primary ID: 009
RENONMED (UDI 009)
Manufactured by Zhejiang Renon Medical Instrument Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RENONMED - Primary ID 009
Device Regulatory Overview
The RENONMED (Model/Catalog Number: 009) is a medical device manufactured by Zhejiang Renon Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification KDT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 009
- Product Code / EMDN
- KDT
- Device Name
- Database Sync Date
- 2026-08-09 09:18:23
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 RENONMED?
The registered manufacturer of record for RENONMED is Zhejiang Renon Medical Instrument Co., Ltd..
What is the Primary UDI-DI identifier for RENONMED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 009.
What classification code is assigned to this device?
This device is registered under product classification code KDT.
Similar Classification Devices (KDT)
Other Devices by Zhejiang Renon Medical Instrument Co., Ltd.
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