gudid
Primary ID: RM0752754
Bard (UDI RM0752754)
Manufactured by Sterilance Medical (Suzhou) Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bard - Primary ID RM0752754
Device Regulatory Overview
The Bard (Model/Catalog Number: RM0752754) is a medical device manufactured by Sterilance Medical (Suzhou) Inc.. This product is indexed under FDA Product Code / Category Classification GDX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RM0752754
- Product Code / EMDN
- GDX
- Device Name
- Database Sync Date
- 2026-08-09 09:11:03
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 Bard?
The registered manufacturer of record for Bard is Sterilance Medical (Suzhou) Inc..
What is the Primary UDI-DI identifier for Bard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RM0752754.
What classification code is assigned to this device?
This device is registered under product classification code GDX.
Similar Classification Devices (GDX)
Other Devices by Sterilance Medical (Suzhou) Inc.
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