gudid
Primary ID: 10430
ESR Control (UDI 10430)
Manufactured by DIESSE DIAGNOSTICA SENESE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ESR Control - Primary ID 10430
Device Regulatory Overview
The ESR Control (Model/Catalog Number: 10430) is a medical device manufactured by DIESSE DIAGNOSTICA SENESE SPA. This product is indexed under FDA Product Code / Category Classification JPH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10430
- Product Code / EMDN
- JPH
- Device Name
- Database Sync Date
- 2026-08-09 09:04:33
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 ESR Control?
The registered manufacturer of record for ESR Control is DIESSE DIAGNOSTICA SENESE SPA.
What is the Primary UDI-DI identifier for ESR Control?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10430.
What classification code is assigned to this device?
This device is registered under product classification code JPH.
Similar Classification Devices (JPH)
Other Devices by DIESSE DIAGNOSTICA SENESE SPA
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