eudamed_udi
Primary ID: D-074924PT
ZS Lucovital Cough&Throat (UDI D-074924PT)
Manufactured by PK Benelux BV
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZS Lucovital Cough&Throat - Primary ID D-074924PT
Device Regulatory Overview
The ZS Lucovital Cough&Throat (Model/Catalog Number: 074924) is a medical device manufactured by PK Benelux BV. This product is indexed under FDA Product Code / Category Classification R028099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 074924
- Product Code / EMDN
- R028099
- Device Name
- Cough&Throat
- Database Sync Date
- 2026-08-09 16:28:47
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 ZS Lucovital Cough&Throat?
The registered manufacturer of record for ZS Lucovital Cough&Throat is PK Benelux BV.
What is the Primary UDI-DI identifier for ZS Lucovital Cough&Throat?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-074924PT.
What classification code is assigned to this device?
This device is registered under product classification code R028099.
Similar Classification Devices (R028099)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint