gudid
Primary ID: RS
IOB (UDI RS)
Manufactured by Jiangmen Dacheng Medical Equipment Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IOB - Primary ID RS
Device Regulatory Overview
The IOB (Model/Catalog Number: RS) is a medical device manufactured by Jiangmen Dacheng Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification DWJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RS
- Product Code / EMDN
- DWJ
- Device Name
- Database Sync Date
- 2026-08-09 09:05:25
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 IOB?
The registered manufacturer of record for IOB is Jiangmen Dacheng Medical Equipment Co., Ltd..
What is the Primary UDI-DI identifier for IOB?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RS.
What classification code is assigned to this device?
This device is registered under product classification code DWJ.
Similar Classification Devices (DWJ)
Other Devices by Jiangmen Dacheng Medical Equipment Co., Ltd.
Programmatic Export
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JSON API Endpoint