eudamed_udi
Primary ID: 08436617644672
PHYSIOMUCOL (UDI 08436617644672)
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 PHYSIOMUCOL - Primary ID 08436617644672
Device Regulatory Overview
The PHYSIOMUCOL (Model/Catalog Number: PL0235_140) 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
- PL0235_140
- Product Code / EMDN
- Q030199
- Device Name
- COUGH SYRUP HEDERA
- Database Sync Date
- 2026-08-09 16:46:03
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 PHYSIOMUCOL?
The registered manufacturer of record for PHYSIOMUCOL is STE PHARMACEUTICALS, S.L.U.
What is the Primary UDI-DI identifier for PHYSIOMUCOL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436617644672.
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
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