eudamed_udi
Primary ID: 08057729510398
HYLAN ULTRA (UDI 08057729510398)
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 HYLAN ULTRA - Primary ID 08057729510398
Device Regulatory Overview
The HYLAN ULTRA (Model/Catalog Number: DT/01/DT/008) 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/008
- Product Code / EMDN
- Q0299
- Device Name
- DT/01/DT/008
- Database Sync Date
- 2026-08-09 16:59:02
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of HYLAN ULTRA?
The registered manufacturer of record for HYLAN ULTRA is C.O.C. FARMACEUTICI S.R.L..
What is the Primary UDI-DI identifier for HYLAN ULTRA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057729510398.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint