eudamed_udi
Primary ID: 05900779759404
HYALUHERB KROPLE DO OCZU (UDI 05900779759404)
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 HYALUHERB KROPLE DO OCZU - Primary ID 05900779759404
Device Regulatory Overview
The HYALUHERB KROPLE DO OCZU (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 17:03:23
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 HYALUHERB KROPLE DO OCZU?
The registered manufacturer of record for HYALUHERB KROPLE DO OCZU is C.O.C. FARMACEUTICI S.R.L..
What is the Primary UDI-DI identifier for HYALUHERB KROPLE DO OCZU?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900779759404.
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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