gudid
Primary ID: 81200
CHORUS TRIO (UDI 81200)
Manufactured by DIESSE DIAGNOSTICA SENESE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHORUS TRIO - Primary ID 81200
Device Regulatory Overview
The CHORUS TRIO (Model/Catalog Number: 81200) is a medical device manufactured by DIESSE DIAGNOSTICA SENESE SPA. This product is indexed under FDA Product Code / Category Classification JJE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 81200
- Product Code / EMDN
- JJE
- 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 CHORUS TRIO?
The registered manufacturer of record for CHORUS TRIO is DIESSE DIAGNOSTICA SENESE SPA.
What is the Primary UDI-DI identifier for CHORUS TRIO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 81200.
What classification code is assigned to this device?
This device is registered under product classification code JJE.
Similar Classification Devices (JJE)
Other Devices by DIESSE DIAGNOSTICA SENESE SPA
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