eudamed_udi
Primary ID: 08033959760338
I-QURE UD (UDI 08033959760338)
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 I-QURE UD - Primary ID 08033959760338
Device Regulatory Overview
The I-QURE UD (Model/Catalog Number: DT/01/DT/003) 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/003
- Product Code / EMDN
- Q0299
- Device Name
- DT/01/DT/003
- Database Sync Date
- 2026-08-09 17:11:35
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 I-QURE UD?
The registered manufacturer of record for I-QURE UD is C.O.C. FARMACEUTICI S.R.L..
What is the Primary UDI-DI identifier for I-QURE UD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033959760338.
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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