eudamed_udi
Primary ID: 06417927103464
IIRIS (UDI 06417927103464)
Manufactured by C.O.C. FARMACEUTICI S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IIRIS - Primary ID 06417927103464
Device Regulatory Overview
The IIRIS (Model/Catalog Number: DT/01/DT/010) is a medical device manufactured by C.O.C. FARMACEUTICI S.R.L.. This product is indexed under FDA Product Code / Category Classification Q0299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DT/01/DT/010
- Product Code / EMDN
- Q0299
- Device Name
- DT/01/DT/010
- Database Sync Date
- 2026-08-09 16:49:49
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 IIRIS?
The registered manufacturer of record for IIRIS is C.O.C. FARMACEUTICI S.R.L..
What is the Primary UDI-DI identifier for IIRIS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06417927103464.
What classification code is assigned to this device?
This device is registered under product classification code Q0299.
Similar Classification Devices (Q0299)
Other Devices by C.O.C. FARMACEUTICI S.R.L.
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