eudamed_udi
Primary ID: 08595566420888
DR.MAX OCNÍ KAPKY (UDI 08595566420888)
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 DR.MAX OCNÍ KAPKY - Primary ID 08595566420888
Device Regulatory Overview
The DR.MAX OCNÍ KAPKY (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 16:58:16
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 DR.MAX OCNÍ KAPKY?
The registered manufacturer of record for DR.MAX OCNÍ KAPKY is C.O.C. FARMACEUTICI S.R.L..
What is the Primary UDI-DI identifier for DR.MAX OCNÍ KAPKY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08595566420888.
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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