gudid
Primary ID: D970 DIDECO AVANT R
RESERVOIR (UDI D970 DIDECO AVANT R)
Manufactured by SORIN GROUP ITALIA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RESERVOIR - Primary ID D970 DIDECO AVANT R
Device Regulatory Overview
The RESERVOIR (Model/Catalog Number: D970 DIDECO AVANT R) is a medical device manufactured by SORIN GROUP ITALIA SRL. This product is indexed under FDA Product Code / Category Classification JOW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D970 DIDECO AVANT R
- Product Code / EMDN
- JOW
- Device Name
- Database Sync Date
- 2026-08-09 09:05:05
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 RESERVOIR?
The registered manufacturer of record for RESERVOIR is SORIN GROUP ITALIA SRL.
What is the Primary UDI-DI identifier for RESERVOIR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D970 DIDECO AVANT R.
What classification code is assigned to this device?
This device is registered under product classification code JOW.
Similar Classification Devices (JOW)
Other Devices by SORIN GROUP ITALIA SRL
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