eudamed_udi
Primary ID: 08436617643996
PHYSIO TUSS (UDI 08436617643996)
Manufactured by STE PHARMACEUTICALS, S.L.U
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PHYSIO TUSS - Primary ID 08436617643996
Device Regulatory Overview
The PHYSIO TUSS (Model/Catalog Number: PL0227_120) is a medical device manufactured by STE PHARMACEUTICALS, S.L.U. This product is indexed under FDA Product Code / Category Classification Q030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PL0227_120
- Product Code / EMDN
- Q030199
- Device Name
- COUGH SYRUP GRINDELIA PRESERVATIVE FREE
- Database Sync Date
- 2026-08-09 16:29:38
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 PHYSIO TUSS?
The registered manufacturer of record for PHYSIO TUSS is STE PHARMACEUTICALS, S.L.U.
What is the Primary UDI-DI identifier for PHYSIO TUSS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436617643996.
What classification code is assigned to this device?
This device is registered under product classification code Q030199.
Similar Classification Devices (Q030199)
Other Devices by STE PHARMACEUTICALS, S.L.U
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint