gudid
Primary ID: 6F DUAL PH.I.S.I.O.
INSPIRE (UDI 6F DUAL PH.I.S.I.O.)
Manufactured by SORIN GROUP ITALIA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INSPIRE - Primary ID 6F DUAL PH.I.S.I.O.
Device Regulatory Overview
The INSPIRE (Model/Catalog Number: 6F DUAL PH.I.S.I.O.) is a medical device manufactured by SORIN GROUP ITALIA SRL. This product is indexed under FDA Product Code / Category Classification DTZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6F DUAL PH.I.S.I.O.
- Product Code / EMDN
- DTZ
- 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 INSPIRE?
The registered manufacturer of record for INSPIRE is SORIN GROUP ITALIA SRL.
What is the Primary UDI-DI identifier for INSPIRE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6F DUAL PH.I.S.I.O..
What classification code is assigned to this device?
This device is registered under product classification code DTZ.
Similar Classification Devices (DTZ)
Other Devices by SORIN GROUP ITALIA SRL
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