gudid
Primary ID: 81220
CHORUS TRIO RAS (UDI 81220)
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 RAS - Primary ID 81220
Device Regulatory Overview
The CHORUS TRIO RAS (Model/Catalog Number: 81220) 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
- 81220
- 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 RAS?
The registered manufacturer of record for CHORUS TRIO RAS is DIESSE DIAGNOSTICA SENESE SPA.
What is the Primary UDI-DI identifier for CHORUS TRIO RAS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 81220.
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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