NOVATIV VISION VISODROP HA+ (UDI 05908288961448)
Manufactured by C.O.C. FARMACEUTICI S.R.L.
Device Regulatory Overview
The NOVATIV VISION VISODROP HA+ (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 17:21:08
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 NOVATIV VISION VISODROP HA+?
The registered manufacturer of record for NOVATIV VISION VISODROP HA+ is C.O.C. FARMACEUTICI S.R.L..
What is the Primary UDI-DI identifier for NOVATIV VISION VISODROP HA+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05908288961448.
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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